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Novel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of Fallot
  • 期刊名称：DNA Cell Biol
  • 时间：2012.11.11
  • 页码：1610-1617
  • 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： Yang YQ|Luo XJ|Xin YF|Liu Y|Liu ZM|Wang Q|Li RG|Fang WY|Wang XZ|
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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A novel GATA6 mutation associated with congenital ventricular septal defect
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PITX2c loss-of-function mutations responsible for congenital atrial septal defects
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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