Functional characterization of SCN1A sodium channel mutations associated with severe myoclonic epilepsy of infancy (SMEI)

被引：0
|
作者：
Rhodes, TH
Lossin, C
Wang, DW
Vanoye, CG
George, AL
机构：
[1] Vanderbilt Univ, Div Med Genet, Nashville, TN USA
[2] Vanderbilt Univ, Dept Pharmacol, Nashville, TN USA
来源：
BIOPHYSICAL JOURNAL | 2004年 / 86卷 / 01期
关键词：
D O I：
暂无
中图分类号：
Q6 [生物物理学];
学科分类号：
071011 ;
摘要：
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页码：424A / 424A
页数：1
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