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)-Reference-Cited by-同舟云学术

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)

Published:2021-01-09 Issue:2 Volume:11 Page:375-385
ISSN:2211-5463
Container-title:FEBS Open Bio
language:en
Short-container-title:FEBS Open Bio

Author:

Peng Jiayu¹,Wang Qingjie¹,Meng Zhuo¹,Wang Jian¹,Zhou Yue¹,Zhou Shuang¹,Song Wenting²,Chen Sun¹,Chen Alex F.³⁴,Sun Kun¹^ORCID

Affiliation:

1. Department of Pediatric Cardiology Xinhua Hospital School of Medicine Shanghai Jiao Tong University Shanghai China

2. Department of Pediatric Cardiology The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University Zhejiang China

3. Institute of Cardiovascular Development and Regeneration Xinhua Hospital School of Medicine Shanghai Jiao Tong University Shanghai China

4. Department of Cardiology Xinhua Hospital School of Medicine Shanghai Jiao Tong University Shanghai China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Biochemistry, Genetics and Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/2211-5463.13044

Reference39 articles.

1. Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia

2. Congenital Heart Surgery Nomenclature and Database Project: pulmonary atresia—ventricular septal defect

3. Identification of Rare Copy Number Variants Associated With Pulmonary Atresia With Ventricular Septal Defect

4. Congenital heart disease in 37,294 births in Tunisia: birth prevalence and mortality rate

5. The Congenital Heart Disease Genetic Network Study

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