Functional characterization of human SCN1A mutations associated with familial epilepsy.

被引：0
|
作者：
Lossin, C [1 ]
Rhodes, TH [1 ]
Vanoye, CG [1 ]
Wang, DW [1 ]
George, AL [1 ]
机构：
[1] Vanderbilt Univ, Nashville, TN 37232 USA
来源：
BIOPHYSICAL JOURNAL | 2003年 / 84卷 / 02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：
引用
收藏
页码：217A / 218A
页数：2
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