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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Int J Med Sci
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Ivyspring International Publisher 2017
Assuntos:
Research Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5436474/
https://ncbi.nlm.nih.gov/pubmed/28553164
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7150/ijms.17834
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados