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Showing articles 0 to 2 of 2 Filter Applied: developmental retardation (Click to remove) Zorevunersen in Children and Adolescents with Dravet Syndrome NEJM 394:969-982, Laux,L.,et al, 2026 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Showing articles 0 to 2 of 2