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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

Document Type

Journal

Author

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

Source

NEUROLOGIA I NEUROCHIRURGIA POLSKA; 2015, 49 4, p258-p266, 9p.

Subject

Language

English

ISSN

00283843

Online Access

Full Text (ScienceDirect 종량제) Full Text (ProQuest Central) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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