From focal epilepsy to Dravet syndrome – Heterogeneity of...

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

Hoffman-Zacharska, Dorota, Szczepanik, Elżbieta, Terczynska, Iwona, Goszczanska-Ciuchta, Alicja, Zalewska-Miszkurka, Zofia, Tataj, Renata, Bal, Jerzy
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Volume:
49
Language:
english
Journal:
Neurologia i Neurochirurgia Polska
DOI:
10.1016/j.pjnns.2015.06.006
Date:
July, 2015
File:
PDF, 614 KB
english, 2015
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