The p.L218P variant in WDR83 disrupts neuronal development, leading to neurodevelopmental disorderHidenori Tabata(Aichi Developmental Disability Center), Koh‐ichi Nagata(Aichi Human Service Center)Scientific ReportsDecember 11, 202510.1038/s41598-025-31794-5Cited by 0SaveCiteExport RISWatch citationsRelated PapersSIL1, a causative cochaperone gene of Marinesco‐Sjögren syndrome, plays an essential role in establishing the architecture of the developing cerebral cortex|EMBO Molecular Medicine|2014|38A Pleiotropic and Functionally Divergent RAC3 Variant Disrupts Neurodevelopment and Impacts Organogenesis|Cells|2025|0