Referenced in: none

Automatically associated channels: Nav1.1

Title: From focal epilepsy to Dravet syndrome--Heterogeneity of the phenotype due to SCN1A mutations of the p.Arg1596 amino acid residue in the Nav1.1 subunit.

Authors: Dorota Hoffman-Zacharska, Elzbieta Szczepanik, Iwona Terczynska, Alicja Goszczanska-Ciuchta, Zofia Zalewska-Miszkurka, Renata Tataj, Jerzy Bal

Journal, date & volume: Neurol. Neurochir. Pol., 2015 , 49, 258-66

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/26188943

Abstract