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De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

Wdr37 Are AssociatedMendelian DisorderGenetic DisorderGeneticsDe Novo VariantsNeurologyNeuroscienceDisease Gene IdentificationNeuropathologyMedicineVariant InterpretationNeurogenetics