Rare predicted deleterious FEZF2 variants are associated with a neurodevelopmental phenotype.

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Bibliographic Details
Title: Rare predicted deleterious FEZF2 variants are associated with a neurodevelopmental phenotype.
Authors: Garber A; Department of Pediatrics, Columbia University, New York, New York, USA., Weingarten LS; Department of Pediatrics, Columbia University, New York, New York, USA., Abreu NJ; Department of Neurology, NYU Grossman School of Medicine, New York, New York, USA., Elloumi HZ; GeneDx, Gaithersburg, Maryland, USA., Haack T; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany., Hildebrant C; Department of Pediatrics, University of North Carolina, Chapel Hill, North Carolina, USA., Martínez-Gil N; Department of Clinical and Molecular Genetics, Vall d'Hebron University Hospital, Barcelona, Spain.; Medical Genetics Group, Vall d'Hebron Research Institute, Barcelona, Spain., Mathews J; Department of Pediatrics, University of North Carolina, Chapel Hill, North Carolina, USA., Müller AJ; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany., Valenzuela Palafoll I; Department of Clinical and Molecular Genetics, Vall d'Hebron University Hospital, Barcelona, Spain.; Medical Genetics Group, Vall d'Hebron Research Institute, Barcelona, Spain., Steigerwald C; Department of Neurology, NYU Grossman School of Medicine, New York, New York, USA., Chung WK; Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2024 Jul; Vol. 194 (7), pp. e63578. Date of Electronic Publication: 2024 Feb 29.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:1552-4833
DOI:10.1002/ajmg.a.63578