A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation

Author： Huang Ri-Tai   Xue Song   Xu Ying-Jia   Zhou Min   Yang Yi-Qing  

Publisher： Spandidos Publications

ISSN： 1107-3756

Source： International Journal of Molecular Medicine, Vol.31, Iss.5, 2013-05, pp. : 1119-1126

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Novel GATA6 loss-of-function mutation responsible for familial atrial fibrillation

By        

International Journal of Molecular Medicine, Vol. 30, Iss. 4, 2012-01 ,pp. : 783-790

Spandidos Publications

Access to resources Recommend Favorite

A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias

By  

International Journal of Molecular Medicine, Vol. 35, Iss. 2, 2015-01 ,pp. : 478-486

Spandidos Publications

Access to resources Recommend Favorite

A novel GATA4 loss-of-function mutation responsible for familial dilated cardiomyopathy

By                  

International Journal of Molecular Medicine, Vol. 33, Iss. 3, 2014-01 ,pp. : 654-660

Spandidos Publications

Access to resources Recommend Favorite

A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation

By                

International Journal of Molecular Medicine, Vol. 31, Iss. 1, 2013-01 ,pp. : 43-50

Spandidos Publications

Access to resources Recommend Favorite

NKX2-6 mutation predisposes to familial atrial fibrillation

By  

International Journal of Molecular Medicine, Vol. 34, Iss. 6, 2014-01 ,pp. : 1581-1590

Spandidos Publications

Access to resources Recommend Favorite