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

Congenital heart disease (CHD), the most common form of developmental abnormality in humans, remains a leading cause of morbidity and mortality in neonates. Genetic defects have been recognized as the predominant causes of CHD. Nevertheless, CHD is of substantial genetic heterogeneity and the geneti...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436474/
https://www.ncbi.nlm.nih.gov/pubmed/28553164
http://dx.doi.org/10.7150/ijms.17834

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436474/
https://www.ncbi.nlm.nih.gov/pubmed/28553164
http://dx.doi.org/10.7150/ijms.17834

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