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MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects.

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Title: MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects.
Authors: Coursimault J; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France., Guerrot AM; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France., Morrow MM; GeneDx, Gaithersburg, 20877 MD, USA., Schramm C; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France., Zamora FM; GeneDx, Gaithersburg, 20877 MD, USA., Shanmugham A; GeneDx, Gaithersburg, 20877 MD, USA., Liu S; GeneDx, Gaithersburg, 20877 MD, USA., Zou F; GeneDx, Gaithersburg, 20877 MD, USA., Bilan F; Service de Génétique, Centre Hospitalier Universitaire de Poitiers, BP577, 86021, Poitiers, France., Le Guyader G; Service de Génétique, Centre Hospitalier Universitaire de Poitiers, BP577, 86021, Poitiers, France., Bruel AL; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France., Denommé-Pichon AS; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France., Faivre L; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Centre de Référence Anomalies du Développement et Syndromes Malformatifs de l'Inter-Région est, FHU TRANSLAD, CHU Dijon-Bourgogne, Dijon, France., Tran Mau-Them F; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France., Tessarech M; Service de Génétique Médicale, CHU d'Angers, Angers, France., Colin E; Service de Génétique Médicale, CHU d'Angers, Angers, France.; Univ Angers, [CHU Angers], INSERM, CNRS, MITOVASC, ICAT, 49000, Angers, SFR, France., El Chehadeh S; Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace (IGMA), Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, Strasbourg, France., Gérard B; Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace (IGMA), Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, Strasbourg, France., Schaefer E; Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace (IGMA), Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, Strasbourg, France., Cogne B; Service de Génétique Médicale, CHU Nantes, Nantes, France., Isidor B; Service de Génétique Médicale, CHU Nantes, Nantes, France., Nizon M; Service de Génétique Médicale, CHU Nantes, Nantes, France., Doummar D; Hôpital Trousseau, APHP.Sorbonne Université, Service de Neuropédiatrie, Paris, France., Valence S; Hôpital Trousseau, APHP.Sorbonne Université, Service de Neuropédiatrie, Paris, France., Héron D; Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière-Hôpital Trousseau Centre de Référence Déficiences Intellectuelles de Causes Rares, APHP.Sorbonne Université, Paris, France., Keren B; Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière-Hôpital Trousseau Centre de Référence Déficiences Intellectuelles de Causes Rares, APHP.Sorbonne Université, Paris, France., Mignot C; Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière-Hôpital Trousseau Centre de Référence Déficiences Intellectuelles de Causes Rares, APHP.Sorbonne Université, Paris, France., Coutton C; Genetic Epigenetic and Therapies of Infertility, Institute for Advanced Biosciences, UMR 5309, CNRS, Université Grenoble Alpes, Inserm U1209, Grenoble, France., Devillard F; Service de Génétique et Procréation, CHU Grenoble Alpes, Grenoble, France., Alaix AS; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France., Amiel J; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France., Colleaux L; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France., Munnich A; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France., Poirier K; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France., Rio M; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France., Rondeau S; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France., Barcia G; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France., Callewaert B; Center for Medical Genetics, Department of Biomolecular Medicine, Ghent University Hospital, Ghent University, Ghent, Belgium., Dheedene A; Center for Medical Genetics, Department of Biomolecular Medicine, Ghent University Hospital, Ghent University, Ghent, Belgium., Kumps C; Center for Medical Genetics, Department of Biomolecular Medicine, Ghent University Hospital, Ghent University, Ghent, Belgium., Vergult S; Center for Medical Genetics, Department of Biomolecular Medicine, Ghent University Hospital, Ghent University, Ghent, Belgium., Menten B; Center for Medical Genetics, Department of Biomolecular Medicine, Ghent University Hospital, Ghent University, Ghent, Belgium., Chung WK; Columbia University Irving Medical Center, New York, NY, USA., Hernan R; Columbia University Irving Medical Center, New York, NY, USA., Larson A; School of Medicine and Children's Hospital, University of Colorado, Aurora, CO, USA., Nori K; School of Medicine and Children's Hospital, University of Colorado, Aurora, CO, USA., Stewart S; School of Medicine and Children's Hospital, University of Colorado, Aurora, CO, USA., Wheless J; Division of Pediatric Neurology, University of Tennessee, Health Science Center, Memphis, USA., Kresge C; Division of Clinical Genetics, Rutgers New Jersey Medical School, Newark, USA., Pletcher BA; Division of Clinical Genetics, Rutgers New Jersey Medical School, Newark, USA., Caumes R; Université de Lille, CHU de Lille, Clinique de Génétique « Guy Fontaine », EA7364 RADEMEF-59000, Lille, France., Smol T; Université de Lille, CHU de Lille, Institut de Génétique Médicale, EA7364 RADEMEF-59000, Lille, France., Sigaudy S; Département de Génétique Médicale, Hôpital Timone Enfant, Marseille, France., Coubes C; Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, CHU Montpellier, Montpellier, France., Helm M; Department of Pediatrics, Division of Genetics. Portland, Maine Medical Center, Maine, USA., Smith R; Department of Pediatrics, Division of Genetics. Portland, Maine Medical Center, Maine, USA., Morrison J; Arnold Palmer Hospital, Orlando Health, Orlando, FL, USA., Wheeler PG; Arnold Palmer Hospital, Orlando Health, Orlando, FL, USA., Kritzer A; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA., Jouret G; National Center of Genetics (NCG), Laboratoire National de Santé (LNS), L-3555, Dudelange, Luxembourg., Afenjar A; Centre de Référence Malformations et Maladies Congénitales du Cervelet et Déficiences Intellectuelles de Causes Rares, Département de Génétique et Embryologie Médicale, APHP. Sorbonne Université, Hôpital Trousseau, 75012, Paris, France., Deleuze JF; Centre National de Recherche en Génomique Humaine (CNRGH), Université Paris-Saclay, CEA, 91057, Evry, France., Olaso R; Centre National de Recherche en Génomique Humaine (CNRGH), Université Paris-Saclay, CEA, 91057, Evry, France., Boland A; Centre National de Recherche en Génomique Humaine (CNRGH), Université Paris-Saclay, CEA, 91057, Evry, France., Poitou C; Service de Nutrition, Hôpital de la Pitié Salpêtrière - AP-HP, Paris, France., Frebourg T; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France., Houdayer C; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France., Saugier-Veber P; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France., Nicolas G; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France., Lecoquierre F; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France. francois.lecoquierre@chu-rouen.fr.
Source: Human genetics [Hum Genet] 2022 Jan; Vol. 141 (1), pp. 65-80. Date of Electronic Publication: 2021 Nov 08.
Publication Type: Journal Article
Journal Info: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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Items – Name: Title
  Label: Title
  Group: Ti
  Data: MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Coursimault+J%22">Coursimault J</searchLink>; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France.<br /><searchLink fieldCode="AU" term="%22Guerrot+AM%22">Guerrot AM</searchLink>; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France.<br /><searchLink fieldCode="AU" term="%22Morrow+MM%22">Morrow MM</searchLink>; GeneDx, Gaithersburg, 20877 MD, USA.<br /><searchLink fieldCode="AU" term="%22Schramm+C%22">Schramm C</searchLink>; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France.<br /><searchLink fieldCode="AU" term="%22Zamora+FM%22">Zamora FM</searchLink>; GeneDx, Gaithersburg, 20877 MD, USA.<br /><searchLink fieldCode="AU" term="%22Shanmugham+A%22">Shanmugham A</searchLink>; GeneDx, Gaithersburg, 20877 MD, USA.<br /><searchLink fieldCode="AU" term="%22Liu+S%22">Liu S</searchLink>; GeneDx, Gaithersburg, 20877 MD, USA.<br /><searchLink fieldCode="AU" term="%22Zou+F%22">Zou F</searchLink>; GeneDx, Gaithersburg, 20877 MD, USA.<br /><searchLink fieldCode="AU" term="%22Bilan+F%22">Bilan F</searchLink>; Service de Génétique, Centre Hospitalier Universitaire de Poitiers, BP577, 86021, Poitiers, France.<br /><searchLink fieldCode="AU" term="%22Le+Guyader+G%22">Le Guyader G</searchLink>; Service de Génétique, Centre Hospitalier Universitaire de Poitiers, BP577, 86021, Poitiers, France.<br /><searchLink fieldCode="AU" term="%22Bruel+AL%22">Bruel AL</searchLink>; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Denommé-Pichon+AS%22">Denommé-Pichon AS</searchLink>; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Faivre+L%22">Faivre L</searchLink>; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Centre de Référence Anomalies du Développement et Syndromes Malformatifs de l'Inter-Région est, FHU TRANSLAD, CHU Dijon-Bourgogne, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Tran+Mau-Them+F%22">Tran Mau-Them F</searchLink>; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Tessarech+M%22">Tessarech M</searchLink>; Service de Génétique Médicale, CHU d'Angers, Angers, France.<br /><searchLink fieldCode="AU" term="%22Colin+E%22">Colin E</searchLink>; Service de Génétique Médicale, CHU d'Angers, Angers, France.; Univ Angers, [CHU Angers], INSERM, CNRS, MITOVASC, ICAT, 49000, Angers, SFR, France.<br /><searchLink fieldCode="AU" term="%22El+Chehadeh+S%22">El Chehadeh S</searchLink>; Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace (IGMA), Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, Strasbourg, France.<br /><searchLink fieldCode="AU" term="%22Gérard+B%22">Gérard B</searchLink>; Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace (IGMA), Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, Strasbourg, France.<br /><searchLink fieldCode="AU" term="%22Schaefer+E%22">Schaefer E</searchLink>; Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace (IGMA), Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, Strasbourg, France.<br /><searchLink fieldCode="AU" term="%22Cogne+B%22">Cogne B</searchLink>; Service de Génétique Médicale, CHU Nantes, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Isidor+B%22">Isidor B</searchLink>; Service de Génétique Médicale, CHU Nantes, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Nizon+M%22">Nizon M</searchLink>; Service de Génétique Médicale, CHU Nantes, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Doummar+D%22">Doummar D</searchLink>; Hôpital Trousseau, APHP.Sorbonne Université, Service de Neuropédiatrie, Paris, France.<br /><searchLink fieldCode="AU" term="%22Valence+S%22">Valence S</searchLink>; Hôpital Trousseau, APHP.Sorbonne Université, Service de Neuropédiatrie, Paris, France.<br /><searchLink fieldCode="AU" term="%22Héron+D%22">Héron D</searchLink>; Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière-Hôpital Trousseau Centre de Référence Déficiences Intellectuelles de Causes Rares, APHP.Sorbonne Université, Paris, France.<br /><searchLink fieldCode="AU" term="%22Keren+B%22">Keren B</searchLink>; Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière-Hôpital Trousseau Centre de Référence Déficiences Intellectuelles de Causes Rares, APHP.Sorbonne Université, Paris, France.<br /><searchLink fieldCode="AU" term="%22Mignot+C%22">Mignot C</searchLink>; Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière-Hôpital Trousseau Centre de Référence Déficiences Intellectuelles de Causes Rares, APHP.Sorbonne Université, Paris, France.<br /><searchLink fieldCode="AU" term="%22Coutton+C%22">Coutton C</searchLink>; Genetic Epigenetic and Therapies of Infertility, Institute for Advanced Biosciences, UMR 5309, CNRS, Université Grenoble Alpes, Inserm U1209, Grenoble, France.<br /><searchLink fieldCode="AU" term="%22Devillard+F%22">Devillard F</searchLink>; Service de Génétique et Procréation, CHU Grenoble Alpes, Grenoble, France.<br /><searchLink fieldCode="AU" term="%22Alaix+AS%22">Alaix AS</searchLink>; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France.<br /><searchLink fieldCode="AU" term="%22Amiel+J%22">Amiel J</searchLink>; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France.<br /><searchLink fieldCode="AU" term="%22Colleaux+L%22">Colleaux L</searchLink>; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France.<br /><searchLink fieldCode="AU" term="%22Munnich+A%22">Munnich A</searchLink>; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France.<br /><searchLink fieldCode="AU" term="%22Poirier+K%22">Poirier K</searchLink>; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France.<br /><searchLink fieldCode="AU" term="%22Rio+M%22">Rio M</searchLink>; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France.<br /><searchLink fieldCode="AU" term="%22Rondeau+S%22">Rondeau S</searchLink>; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France.<br /><searchLink fieldCode="AU" term="%22Barcia+G%22">Barcia G</searchLink>; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, Paris, France.<br /><searchLink fieldCode="AU" term="%22Callewaert+B%22">Callewaert B</searchLink>; Center for Medical Genetics, Department of Biomolecular Medicine, Ghent University Hospital, Ghent University, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22Dheedene+A%22">Dheedene A</searchLink>; Center for Medical Genetics, Department of Biomolecular Medicine, Ghent University Hospital, Ghent University, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22Kumps+C%22">Kumps C</searchLink>; Center for Medical Genetics, Department of Biomolecular Medicine, Ghent University Hospital, Ghent University, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22Vergult+S%22">Vergult S</searchLink>; Center for Medical Genetics, Department of Biomolecular Medicine, Ghent University Hospital, Ghent University, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22Menten+B%22">Menten B</searchLink>; Center for Medical Genetics, Department of Biomolecular Medicine, Ghent University Hospital, Ghent University, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22Chung+WK%22">Chung WK</searchLink>; Columbia University Irving Medical Center, New York, NY, USA.<br /><searchLink fieldCode="AU" term="%22Hernan+R%22">Hernan R</searchLink>; Columbia University Irving Medical Center, New York, NY, USA.<br /><searchLink fieldCode="AU" term="%22Larson+A%22">Larson A</searchLink>; School of Medicine and Children's Hospital, University of Colorado, Aurora, CO, USA.<br /><searchLink fieldCode="AU" term="%22Nori+K%22">Nori K</searchLink>; School of Medicine and Children's Hospital, University of Colorado, Aurora, CO, USA.<br /><searchLink fieldCode="AU" term="%22Stewart+S%22">Stewart S</searchLink>; School of Medicine and Children's Hospital, University of Colorado, Aurora, CO, USA.<br /><searchLink fieldCode="AU" term="%22Wheless+J%22">Wheless J</searchLink>; Division of Pediatric Neurology, University of Tennessee, Health Science Center, Memphis, USA.<br /><searchLink fieldCode="AU" term="%22Kresge+C%22">Kresge C</searchLink>; Division of Clinical Genetics, Rutgers New Jersey Medical School, Newark, USA.<br /><searchLink fieldCode="AU" term="%22Pletcher+BA%22">Pletcher BA</searchLink>; Division of Clinical Genetics, Rutgers New Jersey Medical School, Newark, USA.<br /><searchLink fieldCode="AU" term="%22Caumes+R%22">Caumes R</searchLink>; Université de Lille, CHU de Lille, Clinique de Génétique « Guy Fontaine », EA7364 RADEMEF-59000, Lille, France.<br /><searchLink fieldCode="AU" term="%22Smol+T%22">Smol T</searchLink>; Université de Lille, CHU de Lille, Institut de Génétique Médicale, EA7364 RADEMEF-59000, Lille, France.<br /><searchLink fieldCode="AU" term="%22Sigaudy+S%22">Sigaudy S</searchLink>; Département de Génétique Médicale, Hôpital Timone Enfant, Marseille, France.<br /><searchLink fieldCode="AU" term="%22Coubes+C%22">Coubes C</searchLink>; Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, CHU Montpellier, Montpellier, France.<br /><searchLink fieldCode="AU" term="%22Helm+M%22">Helm M</searchLink>; Department of Pediatrics, Division of Genetics. Portland, Maine Medical Center, Maine, USA.<br /><searchLink fieldCode="AU" term="%22Smith+R%22">Smith R</searchLink>; Department of Pediatrics, Division of Genetics. Portland, Maine Medical Center, Maine, USA.<br /><searchLink fieldCode="AU" term="%22Morrison+J%22">Morrison J</searchLink>; Arnold Palmer Hospital, Orlando Health, Orlando, FL, USA.<br /><searchLink fieldCode="AU" term="%22Wheeler+PG%22">Wheeler PG</searchLink>; Arnold Palmer Hospital, Orlando Health, Orlando, FL, USA.<br /><searchLink fieldCode="AU" term="%22Kritzer+A%22">Kritzer A</searchLink>; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.<br /><searchLink fieldCode="AU" term="%22Jouret+G%22">Jouret G</searchLink>; National Center of Genetics (NCG), Laboratoire National de Santé (LNS), L-3555, Dudelange, Luxembourg.<br /><searchLink fieldCode="AU" term="%22Afenjar+A%22">Afenjar A</searchLink>; Centre de Référence Malformations et Maladies Congénitales du Cervelet et Déficiences Intellectuelles de Causes Rares, Département de Génétique et Embryologie Médicale, APHP. Sorbonne Université, Hôpital Trousseau, 75012, Paris, France.<br /><searchLink fieldCode="AU" term="%22Deleuze+JF%22">Deleuze JF</searchLink>; Centre National de Recherche en Génomique Humaine (CNRGH), Université Paris-Saclay, CEA, 91057, Evry, France.<br /><searchLink fieldCode="AU" term="%22Olaso+R%22">Olaso R</searchLink>; Centre National de Recherche en Génomique Humaine (CNRGH), Université Paris-Saclay, CEA, 91057, Evry, France.<br /><searchLink fieldCode="AU" term="%22Boland+A%22">Boland A</searchLink>; Centre National de Recherche en Génomique Humaine (CNRGH), Université Paris-Saclay, CEA, 91057, Evry, France.<br /><searchLink fieldCode="AU" term="%22Poitou+C%22">Poitou C</searchLink>; Service de Nutrition, Hôpital de la Pitié Salpêtrière - AP-HP, Paris, France.<br /><searchLink fieldCode="AU" term="%22Frebourg+T%22">Frebourg T</searchLink>; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France.<br /><searchLink fieldCode="AU" term="%22Houdayer+C%22">Houdayer C</searchLink>; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France.<br /><searchLink fieldCode="AU" term="%22Saugier-Veber+P%22">Saugier-Veber P</searchLink>; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France.<br /><searchLink fieldCode="AU" term="%22Nicolas+G%22">Nicolas G</searchLink>; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France.<br /><searchLink fieldCode="AU" term="%22Lecoquierre+F%22">Lecoquierre F</searchLink>; Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, CHU Rouen, Inserm U1245, FHU G4 Génomique, F-76000, Rouen, France. francois.lecoquierre@chu-rouen.fr.
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  Data: <searchLink fieldCode="JN" term="%227613873%22">Human genetics</searchLink> [Hum Genet] 2022 Jan; Vol. 141 (1), pp. 65-80. <i>Date of Electronic Publication: </i>2021 Nov 08.
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      – Code: eng
        Text: English
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      – TitleFull: MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects.
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            – D: 01
              M: 01
              Text: 2022 Jan
              Type: published
              Y: 2022
          Identifiers:
            – Type: issn-electronic
              Value: 1432-1203
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          Titles:
            – TitleFull: Human genetics
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