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Volumn 263, Issue 2, 2016, Pages 334-343

Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia

Author keywords

Ataxia; Channelopathy; Epilepsy; Genetics; Sodium channel

Indexed keywords

ALANINE; ARGININE; GLYCINE; SODIUM CHANNEL; VALINE; SCN2A PROTEIN, HUMAN; SODIUM CHANNEL NAV1.2;

EID: 84957973635     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-015-7984-0     Document Type: Article
Times cited : (79)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.