SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain

标题
SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain
作者
关键词
-
出版物
NEUROLOGY
Volume 75, Issue 16, Pages 1454-1458
出版商
Ovid Technologies (Wolters Kluwer Health)
发表日期
2010-10-19
DOI
10.1212/wnl.0b013e3181f8812e

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