Quinidine Therapy for Lennox-Gastaut Syndrome With KCNT1 Mutation. A Case Report and Literature Review
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DOI: 10.3389/fneur.2019.00064
Abstract: Mutations in the Potassium channel subfamily T member 1 (KCNT1) gene have been reported in a range of epileptic encephalopathies. Here we report the case of a 12-year-old male suffering from multiple types of epileptic… read more here.
Keywords: kcnt1 mutation; lennox gastaut; syndrome kcnt1; gastaut syndrome ... See more keywords