位置：成果数据库 > 期刊 > 期刊详情页
Mutations of the SCN4B-encoded sodium channel beta 4 subunit in familial atrial fibrillation
  • ISSN号：1107-3756
  • 期刊名称：International Journal of Molecular Medicine
  • 时间：2013.7.7
  • 页码：144-150
  • 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： Li RG|Wang Q|Xu YJ|Zhang M|Qu XK|Liu X|Fang WY|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
同项目期刊论文
GATA5 loss-of-function mutations underlie tetralogy of Fallot
A novel GATA4 mutation responsible for congenital ventricular septal defects
Involvement of a novel GATA4 mutation in atrial septal defects
Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation
Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation
A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation
Prevalence and spectrum of GJA5 mutations associated with lone atrial fibrillation
Novel Germline GJA5/Connexin40 Mutations Associated with Lone Atrial Fibrillation Impair Gap Junctio
A novel PITX2c loss-of-function mutation underlies lone atrial fibrillation
Prevalence and spectrum of PITX2c mutations associated with familial atrial fibrillation
GATA4 loss-of-function mutations underlie familial tetralogy of Fallot
Novel GATA6 loss-of-function mutation responsible for familial atrial fibrillation
Novel GATA4 mutations in patients with congenital ventricular septal defects
A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation.
Somatic mutations in the GATA6 gene underlie sporadic tetralogy of Fallot
Novel NKX2-5 mutations responsible for congenital heart disease
Prevalence and spectrum of GATA5 mutations associated with congenital heart disease
GATA5 Loss-of-Function Mutation Responsible for the Congenital Ventriculoseptal Defect
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
Novel GATA4 mutations in lone atrial fibrillation
Mutational spectrum of the GATA5 gene associated with familial atrial fibrillation.
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