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...

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Detalles Bibliográficos
Autores principales: Peng, Jiayu, Wang, Qingjie, Meng, Zhuo, Wang, Jian, Zhou, Yue, Zhou, Shuang, Song, Wenting, Chen, Sun, Chen, Alex F., Sun, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876499/
https://www.ncbi.nlm.nih.gov/pubmed/33211401
http://dx.doi.org/10.1002/2211-5463.13044

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