CASZ1 loss-of-function mutation associated with congenital heart disease-Reference-Cited by-同舟云学术

CASZ1 loss-of-function mutation associated with congenital heart disease

Published:2016-12 Issue:1 Volume:595 Page:62-68
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Huang Ri-Tai,Xue Song,Wang Juan,Gu Jian-Yun,Xu Jia-Hong,Li Yan-Jie,Li Ning,Yang Xiao-Xiao,Liu Hua,Zhang Xiao-Dong,Qu Xin-Kai,Xu Ying-Jia,Qiu Xing-Biao,Li Ruo-Gu,Yang Yi-Qing

Funder

National Natural Science Foundation of China

Basic Research of Shanghai, China

Shanghai Chest Hospital, China

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference60 articles.

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4. Genetic variations of NKX2-5 in sporadic atrial septal defect and ventricular septal defect in Chinese Yunnan population;Cao;Gene,2016

5. A novel mutation of GATA4 (K300T) associated with familial atrial septal defect;Chen;Gene,2016

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