Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.

Mutations inĀ SCN2A, a gene encoding the voltage-gated sodium channel Nav1.2, have been associated with a spectrum of epilepsies and neurodevelopmental disorders.

Brain 140.5 (2017): 1316-1336.
Wolff, Markus, et al.
https://academic.oup.com/brain/article/140/5/1316/3098477