标题
Exome sequencing in Parkinson's disease
作者
关键词
-
出版物
CLINICAL GENETICS
Volume 80, Issue 2, Pages 104-109
出版商
Wiley
发表日期
2011-06-09
DOI
10.1111/j.1399-0004.2011.01722.x
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies
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