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Whole-exome sequencing identify a new mutation of MYH7 in a Chinese family with left ventricular non
  • ISSN号：0378-1119
  • 期刊名称：Gene
  • 时间：2014.12.27
  • 页码：491-496
  • 相关项目：SCN5A突变(D772N和A1656V)致重叠型室性心律失常机制的研究
作者： Daowu Wang|Hongbing Shen|Zhibin Hu|Jiangang Zou|
同期刊论文项目
SCN5A突变(D772N和A1656V)致重叠型室性心律失常机制的研究
期刊论文 15
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