TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus-Reference-Cited by-同舟云学术

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TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus

Published:2017 Issue:4 Volume:14 Page:323-332
ISSN:1449-1907
Container-title:International Journal of Medical Sciences
language:en
Short-container-title:Int. J. Med. Sci.

Author:

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

Publisher

Ivyspring International Publisher

Subject

General Medicine

Cited by 43 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Discovery of BMP10 as a new gene underpinning congenital heart defects;American Journal of Translational Research;2024

2. Human Genetics of Truncus Arteriosus;Advances in Experimental Medicine and Biology;2024

3. Genetics of Common Birth Defects in Newborns;Principles of Neonatology;2024

4. The Tbx20-TLE interaction is essential for the maintenance of the second heart field;Development;2023-10-30

5. TBX20loss-of-function variants in families with left ventricular non-compaction cardiomyopathy;Journal of Medical Genetics;2023-09-01

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