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SCN2A Epileptic Encephalopathy

Prevalence: 1/100000

neurological

Official·OMIM:613721 Official·ORPHA442835

Early infantile epileptic encephalopathy due to SCN2A gene mutations.

Associated Genes

SCN2ASodium Voltage-Gated Channel Alpha Subunit 2

Chromosome 2Autosomal Dominant