Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy
出版年份 2013 全文链接
标题
Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy
作者
关键词
-
出版物
BRAIN
Volume 136, Issue 1, Pages 282-293
出版商
Oxford University Press (OUP)
发表日期
2013-10-24
DOI
10.1093/brain/aws293
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。- Myosin regulatory light chain mutation found in hypertrophic cardiomyopathy patients increases isometric force production in transgenic mice
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