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Novel Germline GJA5/Connexin40 Mutations Associated with Lone Atrial Fibrillation Impair Gap Junctio
  • ISSN号：1059-7794
  • 期刊名称：Human Mutation
  • 时间：2013.4.4
  • 页码：603-609
  • 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： Sun Y|Yang YQ|Gong XQ|Wang XH|Li RG|Tan HW|Liu X|Fang WY|Bai D|
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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Mutations of the SCN4B-encoded sodium channel beta 4 subunit in familial atrial fibrillation
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GATA4 loss-of-function mutation underlies familiai dilated cardiomyopathy
A novel NKX2-5 mutation in familial ventricular septal defect
GATA4 loss-of-function mutations in familial atrial fibrillation
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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
Prevalence and spectrum of GATA6 mutations associated with familial atrial fibrillation
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
Prevalence and spectrum of PITX2c mutations associated with congenital heart disease
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