A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect-Reference-Cited by-同舟云学术

A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect

Published:2018-04 Issue:4 Volume:61 Page:197-203
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Qiao Xiao-Hui,Wang Qian,Wang Juan,Liu Xing-Yuan,Xu Ying-Jia,Huang Ri-Tai,Xue Song,Li Yan-Jie,Zhang Min,Qu Xin-Kai,Li Ruo-Gu,Qiu Xing-Biao,Yang Yi-Qing

Funder

National Natural Science Foundation of China

Key Program for Basic Research of Shanghai, China

Natural Science Foundation of Shanghai

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference72 articles.

1. Rare variants in NR2F2 cause congenital heart defects in humans;Al Turki;Am. J. Hum. Genet.,2014

2. Of mice and men: molecular genetics of congenital heart disease;Andersen;Cell Mol. Life Sci.,2014

3. Genotype-phenotype evaluation of MED13L defects in the light of a novel truncating and a recurrent missense mutation;Asadollahi;Eur. J. Med. Genet.,2017

4. Heart disease and stroke statistics—2017 update: a report from the American Heart Association;Benjamin;Circulation,2017

5. Advances in the genetics of congenital heart disease: a clinician's guide;Blue;J. Am. Coll. Cardiol.,2017

Cited by 28 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Human Genetics of Ventricular Septal Defect;Advances in Experimental Medicine and Biology;2024

2. Genetics of Common Birth Defects in Newborns;Principles of Neonatology;2024

3. Sinus venosus adaptation models prolonged cardiovascular disease and reveals insights into evolutionary transitions of the vertebrate heart;Nature Communications;2023-09-07

4. Maternal body fluid lncRNAs serve as biomarkers to diagnose ventricular septal defect: from amniotic fluid to plasma;Frontiers in Genetics;2023-09-06

5. Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays;European Journal of Human Genetics;2023-07-27