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GATA5 Loss-of-Function Mutation Responsible for the Congenital Ventriculoseptal Defect
  • ISSN号：0172-0643
  • 期刊名称：Pediatric Cardiology
  • 时间：2013.3.3
  • 页码：504-511
  • 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： Wei D|Bao H|Zhou N|Zheng GF|Liu XY|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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GATA6 loss-of-function mutation in atrial fibrillation
Mutation spectrum of the GATA4 gene in patients with idiopathic atrial fibrillation
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
A novel GATA4 loss-of-function mutation associated with congenital ventricular septal defect
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