MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

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Bibliographic Details
Title: MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.
Authors: Shamseldin HE; Department of Translational Genomics, Genomic Medicine Centre of Excellence, King Faisal Specialist Hospital and Research Center, MBC-26, PO BOX 3354, 11211, Riyadh, Saudi Arabia., Marafi D; Department of Pediatrics, Faculty of Medicine, Kuwait University, 13110, Safat, Kuwait.; Department of Pediatrics, Adan Hospital, Ministry of Health, 52700, Hadiya, Kuwait.; Kuwait Medical Genetics Centre, Ministry of Health, 80901, Sulaibikhat, Kuwait., AlMuhaizea M; Neuroscience Centre, King Faisal Specialist Hospital and Research Centre, 11211, Riyadh, Saudi Arabia., Ceolin C'; Program in Developmental and Stem Cell Biology, SickKids Research Institute, Toronto, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, Canada., Abdulwahab F; Department of Translational Genomics, Genomic Medicine Centre of Excellence, King Faisal Specialist Hospital and Research Center, MBC-26, PO BOX 3354, 11211, Riyadh, Saudi Arabia., Alshidi T; Department of Translational Genomics, Genomic Medicine Centre of Excellence, King Faisal Specialist Hospital and Research Center, MBC-26, PO BOX 3354, 11211, Riyadh, Saudi Arabia., Albash B; Kuwait Medical Genetics Centre, Ministry of Health, 80901, Sulaibikhat, Kuwait., Alabdulrazzaq F; Department of Pediatrics, Faculty of Medicine, Kuwait University, 13110, Safat, Kuwait.; Kuwait Institute of Medical Specialization, Sulaibkikhat, P.O. Box: 1793, 13018, Safat, Kuwait., Murthy HR; Program in Developmental and Stem Cell Biology, SickKids Research Institute, Toronto, Canada., Van Gennip JLM; Program in Developmental and Stem Cell Biology, SickKids Research Institute, Toronto, Canada., Harmic IM; Program in Developmental and Stem Cell Biology, SickKids Research Institute, Toronto, Canada., Simonian R; Zebrafish Genetics and Disease Model Core, SickKids Research Institute, Toronto, Canada., Cui X; Zebrafish Genetics and Disease Model Core, SickKids Research Institute, Toronto, Canada., Burgess J; Zebrafish Genetics and Disease Model Core, SickKids Research Institute, Toronto, Canada., Ciruna B; Program in Developmental and Stem Cell Biology, SickKids Research Institute, Toronto, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, Canada., Deshwar AR; Program in Developmental and Stem Cell Biology, SickKids Research Institute, Toronto, Canada. ashish.deshwar@sickkids.ca.; Department of Molecular Genetics, University of Toronto, Toronto, Canada. ashish.deshwar@sickkids.ca.; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Canada. ashish.deshwar@sickkids.ca.; Department of Paediatrics, University of Toronto, Toronto, Canada. ashish.deshwar@sickkids.ca.; Program in Genetics and Genome Biology, SickKids Research Institute, Toronto, Canada. ashish.deshwar@sickkids.ca., Alkuraya FS; Department of Translational Genomics, Genomic Medicine Centre of Excellence, King Faisal Specialist Hospital and Research Center, MBC-26, PO BOX 3354, 11211, Riyadh, Saudi Arabia. falkuraya@liferaomics.com.sa.; Lifera Omics, Innovation Boulevard St., KAFD, Al Aqeeq Dist. KAFD, 4.07, 5th Floor, 13519-3004, Riyadh, Saudi Arabia. falkuraya@liferaomics.com.sa., AlAbdi L; Department of Translational Genomics, Genomic Medicine Centre of Excellence, King Faisal Specialist Hospital and Research Center, MBC-26, PO BOX 3354, 11211, Riyadh, Saudi Arabia. lalabdi@kfshrc.edu.sa.
Source: Scientific reports [Sci Rep] 2026 Jul 15. Date of Electronic Publication: 2026 Jul 15.
Publication Type: Journal Article
Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2045-2322
DOI:10.1038/s41598-026-61907-7