A Novel NKX2.5 Loss-of-Function Mutation Associated With Congenital Bicuspid Aortic Valve-Reference-Cited by-同舟云学术

A Novel NKX2.5 Loss-of-Function Mutation Associated With Congenital Bicuspid Aortic Valve

Published:2014-12 Issue:12 Volume:114 Page:1891-1895
ISSN:0002-9149
Container-title:The American Journal of Cardiology
language:en
Short-container-title:The American Journal of Cardiology

Author:

Qu Xin-Kai,Qiu Xing-Biao,Yuan Fang,Wang Juan,Zhao Cui-Mei,Liu Xing-Yuan,Zhang Xian-Ling,Li Ruo-Gu,Xu Ying-Jia,Hou Xu-Min,Fang Wei-Yi,Liu Xu,Yang Yi-Qing

Funder

National Natural Science Fund

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference28 articles.

1. Heart valve development: regulatory networks in development and disease;Combs;Circ Res,2009

2. Mutations in NOTCH1 cause aortic valve disease;Garg;Nature,2005

3. GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve;Shi;Int J Mol Med,2014

4. Rare GATA5 sequence variants identified in individuals with bicuspid aortic valve;Bonachea;Pediatr Res,2014

5. GATA and Nkx factors synergistically regulate tissue-specific gene expression and development in vivo;Zhang;Development,2007

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