A Novel GNAL Mutation Identified by Whole Exome Sequencing is Associated with Familial Generalized Chorea

被引：0
|
作者：
Parnes, M. S.
Stocco, A. J.
机构：
来源：
ANNALS OF NEUROLOGY | 2014年 / 76卷
关键词：
Case studies/case series; Epilepsy and other paroxysmal disorders; Genetics;
D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
119
引用
收藏
页码：S225 / S226
页数：2
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