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

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

Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neurologia i Neurochirurgia Polska - Volume 49, Issue 4, July–August 2015, Pages 258–266

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