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Phenotypic Characterization of a Novel SCN3A-NDD Mouse Model
SCN3A-related neurodevelopmental disorder (SCN3A-NDD) is caused by heterozygous pathogenic variants in the embryonic voltage-gated sodium channel gene, SCN3A. Patients present with a spectrum of neurological symptoms, with the most prevalent phenotypes being epilepsy, often neonatal-onset and treatm
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