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A novel NKX2-5 mutation in familial ventricular septal defect
  • 期刊名称：Int J Mol Med
  • 时间：2011.3.3
  • 页码：369-375
  • 相关项目：新的家族性房颤致病基因的定位克隆与功能研究
作者： Wang J|Xin YF|Liu XY|Liu ZM|Wang XZ|Yang YQ|
同期刊论文项目
新的家族性房颤致病基因的定位克隆与功能研究
期刊论文 36
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Novel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of Fallot
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A novel GATA6 mutation associated with congenital ventricular septal defect
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孤立性房颤相关SCN4B基因突变谱分析
缝隙连接蛋白40与心房颤动的关系
心脏转录因子GATA4与心房颤动的关系
先天性房间隔缺损相关GATA6基因新突变的识别