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PITX2c loss-of-function mutations responsible for congenital atrial septal defects
  • ISSN号：1449-1907
  • 期刊名称：International Journal of Medical Sciences
  • 时间：2013.10.10
  • 页码：1422-1429
  • 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|Zhao L|Wang J|Zhang W|Li X|Qiu XB|Li RG|Xu YJ|Xu L|
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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Prevalence and spectrum of GATA6 mutations associated with familial atrial fibrillation
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A novel GATA4 loss-of-function 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