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WDR59 Is Mutated in Individuals With Autosomal Recessive Syndromic Dilated Cardiomyopathy.

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Title: WDR59 Is Mutated in Individuals With Autosomal Recessive Syndromic Dilated Cardiomyopathy.
Authors: Alabdi L; Department of Translational Genomics, Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Cogne B; Service de Génétique Médicale, Nantes Université, CHU de Nantes, Nantes, France.; CHU de Nantes, CNRS, INSERM, L'institut du Thorax, F-44000, Nantes Université, Nantes, France.; Laboratoire de Biologie Médicale Multi-Sites SeqOIA (laboratoire-seqoia.fr), Paris, France., Almasood AS; Adult Cardiology Department, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Alsehly A; Pediatric Cardiology Department, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Helaby R; Department of Translational Genomics, Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Maddirevula S; Precision Medicine Laboratory, Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia., Besnard T; Service de Génétique Médicale, Nantes Université, CHU de Nantes, Nantes, France.; CHU de Nantes, CNRS, INSERM, L'institut du Thorax, F-44000, Nantes Université, Nantes, France., Do Souto L; Service de Génétique Médicale, Nantes Université, CHU de Nantes, Nantes, France., Isidor B; Service de Génétique Médicale, Nantes Université, CHU de Nantes, Nantes, France.; CHU de Nantes, CNRS, INSERM, L'institut du Thorax, F-44000, Nantes Université, Nantes, France., Alkuraya FS; Department of Translational Genomics, Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.; Lifera Omics, Riyadh, Saudi Arabia.
Source: Clinical genetics [Clin Genet] 2026 Jul; Vol. 110 (1), pp. 84-89. Date of Electronic Publication: 2026 Feb 19.
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: WDR59 Is Mutated in Individuals With Autosomal Recessive Syndromic Dilated Cardiomyopathy.
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  Data: <searchLink fieldCode="AU" term="%22Alabdi+L%22">Alabdi L</searchLink>; Department of Translational Genomics, Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Cogne+B%22">Cogne B</searchLink>; Service de Génétique Médicale, Nantes Université, CHU de Nantes, Nantes, France.; CHU de Nantes, CNRS, INSERM, L'institut du Thorax, F-44000, Nantes Université, Nantes, France.; Laboratoire de Biologie Médicale Multi-Sites SeqOIA (laboratoire-seqoia.fr), Paris, France.<br /><searchLink fieldCode="AU" term="%22Almasood+AS%22">Almasood AS</searchLink>; Adult Cardiology Department, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Alsehly+A%22">Alsehly A</searchLink>; Pediatric Cardiology Department, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Helaby+R%22">Helaby R</searchLink>; Department of Translational Genomics, Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Maddirevula+S%22">Maddirevula S</searchLink>; Precision Medicine Laboratory, Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Besnard+T%22">Besnard T</searchLink>; Service de Génétique Médicale, Nantes Université, CHU de Nantes, Nantes, France.; CHU de Nantes, CNRS, INSERM, L'institut du Thorax, F-44000, Nantes Université, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Do+Souto+L%22">Do Souto L</searchLink>; Service de Génétique Médicale, Nantes Université, CHU de Nantes, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Isidor+B%22">Isidor B</searchLink>; Service de Génétique Médicale, Nantes Université, CHU de Nantes, Nantes, France.; CHU de Nantes, CNRS, INSERM, L'institut du Thorax, F-44000, Nantes Université, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Alkuraya+FS%22">Alkuraya FS</searchLink>; Department of Translational Genomics, Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.; Lifera Omics, Riyadh, Saudi Arabia.
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  Data: <searchLink fieldCode="JN" term="%220253664%22">Clinical genetics</searchLink> [Clin Genet] 2026 Jul; Vol. 110 (1), pp. 84-89. <i>Date of Electronic Publication: </i>2026 Feb 19.
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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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              Text: 2026 Jul
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