A novel missense mutation inCCDC88Cactivates the JNK pathway and causes a dominant form of spinocerebellar ataxia
出版年份 2014 全文链接
标题
A novel missense mutation inCCDC88Cactivates the JNK pathway and causes a dominant form of spinocerebellar ataxia
作者
关键词
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出版物
JOURNAL OF MEDICAL GENETICS
Volume 51, Issue 9, Pages 590-595
出版商
BMJ
发表日期
2014-07-26
DOI
10.1136/jmedgenet-2014-102333
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias
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