The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant.
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| Title: | The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant. |
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| Authors: | Chatron N; Department of Medical Genetics, Lyon University Hospital and GENDEV team CNRS UMR 5292, INSERM U1028, CRNL, and University Claude Bernard Lyon 1, GHE, Lyon, France., Møller RS; Danish Epilepsy Centre, Dianalund, and University of Southern Denmark, Institute for Regional Health research, Odense, Denmark., Champaigne NL; Greenwood Genetic Center, Greenwood, SC., Schneider AL; Epilepsy Research Centre, Department of Medicine, Austin Health, University of Melbourne, Heidelberg, VIC, Australia., Kuechler A; Institut für Humangenetik, Universitätsklinikum, and Universität Duisburg-Essen, Essen, Germany., Labalme A; Department of Medical Genetics, Lyon University Hospital and GENDEV team CNRS UMR 5292, INSERM U1028, CRNL, and University Claude Bernard Lyon 1, GHE, Lyon, France., Simonet T; Service de Biostatistique-Bioinformatique, Lyon University Hospital, Lyon and CNRS UMR5558, Laboratoire de Biométrie et Biologie Evolutive, Equipe Biostatistique Santé, Villeurbanne, and University Claude Bernard Lyon 1, Lyon, France., Baggett L; Greenwood Genetic Center, Greenwood, SC., Bardel C; Centre de Biotechnologie Cellulaire, Hospices Civils de Lyon, Lyon, and Nerve-Muscle Interactions Team, Institut NeuroMyoGène CNRS UMR 5310-INSERM U1217-Université Claude Bernard Lyon 1, Lyon, France., Kamsteeg EJ; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., Pfundt R; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., Romano C; Oasi Research Institute-IRCCS, Troina, Italy., Aronsson J; Habiliteringscentrum, Ryhov Hospital, Jönköping, Sweden., Alberti A; Oasi Research Institute-IRCCS, Troina, Italy., Vinci M; Oasi Research Institute-IRCCS, Troina, Italy., Miranda MJ; Department of Pediatrics, Pediatric Neurology, Herlev University Hospital, Copenhagen, Denmark., Lacroix A; Department of Pediatrics, Division of Genetic Medicine, University of Washington, Seattle, WA., Marjanovic D; Danish Epilepsy Centre, Dianalund, and University of Southern Denmark, Institute for Regional Health research, Odense, Denmark., des Portes V; Centre de référence « Déficiences Intellectuelles de causes rares », HCL, F-69675, Bron; ISC, CNRS UMR 5304, Bron; Université de Lyon, Lyon, France., Edery P; Department of Medical Genetics, Lyon University Hospital and GENDEV team CNRS UMR 5292, INSERM U1028, CRNL, and University Claude Bernard Lyon 1, GHE, Lyon, France., Wieczorek D; Institut für Humangenetik, Universitätsklinikum, and Universität Duisburg-Essen, Essen, Germany.; Institut für Humangenetik, Universitätsklinikum Essen, Essen, and Institut für Humangenetik, Universitätsklinikum Düsseldorf, Düsseldorf, Germany., Gardella E; Danish Epilepsy Centre, Dianalund, and University of Southern Denmark, Institute for Regional Health research, Odense, Denmark., Scheffer IE; Epilepsy Research Centre, Department of Medicine, Austin Health, University of Melbourne, Heidelberg, VIC, Australia.; Florey Institute of Neuroscience and Mental Health, The University of Melbourne, VIC, Australia.; Department of Paediatrics, Royal Children's Hospital, The University of Melbourne, Parkville, Victoria, Australia., Mefford H; Department of Pediatrics, Division of Genetic Medicine, University of Washington, Seattle, WA., Sanlaville D; Department of Medical Genetics, Lyon University Hospital and GENDEV team CNRS UMR 5292, INSERM U1028, CRNL, and University Claude Bernard Lyon 1, GHE, Lyon, France., Carvill GL; Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL., Lesca G; Department of Medical Genetics, Lyon University Hospital and GENDEV team CNRS UMR 5292, INSERM U1028, CRNL, and University Claude Bernard Lyon 1, GHE, Lyon, France. |
| Source: | Annals of neurology [Ann Neurol] 2018 May; Vol. 83 (5), pp. 926-934. Date of Electronic Publication: 2018 Apr 30. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7707449 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8249 (Electronic) Linking ISSN: 03645134 NLM ISO Abbreviation: Ann Neurol |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1531-8249 |
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| DOI: | 10.1002/ana.25222 |
