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WDTC1 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes.

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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
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  Data: WDTC1 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes.
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  Data: <searchLink fieldCode="AU" term="%22Smith+E%22">Smith E</searchLink>; Genetics and Genomics Program, Baylor College of Medicine, Houston, Texas, USA.<br /><searchLink fieldCode="AU" term="%22Faundes+V%22">Faundes V</searchLink>; Laboratorio de Genética y Enfermedades Metabólicas, Instituto de Nutrición y Tecnología de los Alimentos, Universidad de Chile, Santiago, Chile.<br /><searchLink fieldCode="AU" term="%22Zhao+X%22">Zhao X</searchLink>; Baylor Genetics, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.<br /><searchLink fieldCode="AU" term="%22Zheng+B%22">Zheng B</searchLink>; Nanjing Key Laboratory of Pediatrics, Children's Hospital of Nanjing Medical University, Nanjing, China.<br /><searchLink fieldCode="AU" term="%22Zhang+G%22">Zhang G</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, China.<br /><searchLink fieldCode="AU" term="%22Mao+X%22">Mao X</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Danko+E%22">Danko E</searchLink>; Department of Clinical Genetics, Akron Children's Hospital, Akron, Ohio, USA.<br /><searchLink fieldCode="AU" term="%22Laufman+J%22">Laufman J</searchLink>; Department of Clinical Genetics, Akron Children's Hospital, Akron, Ohio, USA.<br /><searchLink fieldCode="AU" term="%22Besnard+T%22">Besnard T</searchLink>; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France.; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du Thorax, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Isidor+B%22">Isidor B</searchLink>; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France.; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du Thorax, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Cogné+B%22">Cogné B</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Jensson+BÖ%22">Jensson BÖ</searchLink>; Amgen deCODE Genetics, Reykjavik, Iceland.<br /><searchLink fieldCode="AU" term="%22Sulem+TS%22">Sulem TS</searchLink>; Amgen deCODE Genetics, Reykjavik, Iceland.<br /><searchLink fieldCode="AU" term="%22Sulem+P%22">Sulem P</searchLink>; Amgen deCODE Genetics, Reykjavik, Iceland.<br /><searchLink fieldCode="AU" term="%22Rosenfeld+JA%22">Rosenfeld JA</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.<br /><searchLink fieldCode="AU" term="%22Scott+DA%22">Scott DA</searchLink>; Baylor Genetics, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
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  Data: <searchLink fieldCode="JN" term="%220253664%22">Clinical genetics</searchLink> [Clin Genet] 2026 Jul; Vol. 110 (1), pp. 29-35. <i>Date of Electronic Publication: </i>2026 Mar 06.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Munksgaard%22">Munksgaard </searchLink><i>Country of Publication: </i>Denmark <i>NLM ID: </i>0253664 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1399-0004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200099163%22">00099163 </searchLink><i>NLM ISO Abbreviation: </i>Clin Genet <i>Subsets: </i>MEDLINE
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