WDTC1 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes.

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Bibliographic Details
Title: WDTC1 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes.
Authors: Smith E; Genetics and Genomics Program, Baylor College of Medicine, Houston, Texas, USA., Faundes V; Laboratorio de Genética y Enfermedades Metabólicas, Instituto de Nutrición y Tecnología de los Alimentos, Universidad de Chile, Santiago, Chile., Zhao X; Baylor Genetics, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Zheng B; Nanjing Key Laboratory of Pediatrics, Children's Hospital of Nanjing Medical University, Nanjing, China., Zhang G; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, China., Mao X; Department of Medical Genetics, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, China.; National Health Commission Key Laboratory for Birth Defect Research and Prevention, Changsha, Hunan, China., Danko E; Department of Clinical Genetics, Akron Children's Hospital, Akron, Ohio, USA., Laufman J; Department of Clinical Genetics, Akron Children's Hospital, Akron, Ohio, USA., Besnard T; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France.; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du Thorax, Nantes, France., Isidor B; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France.; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du Thorax, Nantes, France., Cogné B; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France.; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du Thorax, Nantes, France.; Laboratoire SeqOIA, Paris, France., Jensson BÖ; Amgen deCODE Genetics, Reykjavik, Iceland., Sulem TS; Amgen deCODE Genetics, Reykjavik, Iceland., Sulem P; Amgen deCODE Genetics, Reykjavik, Iceland., Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Scott DA; Baylor Genetics, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Source: Clinical genetics [Clin Genet] 2026 Jul; Vol. 110 (1), pp. 29-35. Date of Electronic Publication: 2026 Mar 06.
Publication Type: Journal Article
Journal Info: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1399-0004
DOI:10.1111/cge.70160