A de novo mutation of SMYD1 (p. F272L) is responsible for hypertrophic cardiomyopathy in a Chinese patient
发布时间：2019-10-25
点击次数：
影响因子：6.8
发表刊物：Clinical Chemistry and Laboratory Medicine
文献类型：J
卷号：57
期号：4
页面范围：532-539
是否译文：否
发表时间：2019-02-11
收录刊物：SCI
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