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Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation
  • ISSN号：1807-5932
  • 期刊名称：Clinics
  • 时间：2013
  • 页码：777-784
  • 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： Xie, Wen-Hui|Chang, Cheng|Xu, Ying-Jia|Li, Ruo-Gu|Qu, Xin-Kai|Fang, Wei-Yi|Liu, Xu|Yang, Yi-Qing|
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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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