SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases
出版年份 2015 全文链接
标题
SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases
作者
关键词
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出版物
EUROPEAN JOURNAL OF HUMAN GENETICS
Volume 24, Issue 7, Pages 1016-1021
出版商
Springer Nature
发表日期
2015-12-02
DOI
10.1038/ejhg.2015.240
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。- SPG7 mutations are a common cause of undiagnosed ataxia
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