A loss‐of‐function mutation p.T256M in NDRG4 is implicated in the pathogenesis of pulmonary atresia with ventricular septal defect (PA/VSD) and tetralogy of Fallot (TOF)

Pulmonary atresia with ventricular septal defect (PA/VSD) is a rare congenital heart disease (CHD) characterized by a lack of luminal continuity and blood flow from either the right ventricle or the pulmonary artery, together with VSDs. The prevalence of PA/VSD is about 0.2% of live births and appro...

詳細記述

書誌詳細
出版年:FEBS Open Bio
主要な著者: Jiayu Peng, Qingjie Wang, Zhuo Meng, Jian Wang, Yue Zhou, Shuang Zhou, Wenting Song, Sun Chen, Alex F. Chen, Kun Sun
フォーマット: 論文
言語:英語
出版事項: Wiley 2021-02-01
主題:
オンライン・アクセス:https://doi.org/10.1002/2211-5463.13044