Functionally Significant, Rare Transcription Factor Variants in Tetralogy of Fallot-Reference-Cited by-同舟云学术

Functionally Significant, Rare Transcription Factor Variants in Tetralogy of Fallot

Published:2014-08-05 Issue:8 Volume:9 Page:e95453
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Töpf Ana,Griffin Helen R.,Glen Elise,Soemedi Rachel,Brown Danielle L.,Hall Darroch,Rahman Thahira J.,Eloranta Jyrki J.,Jüngst Christoph,Stuart A. Graham,O'Sullivan John,Keavney Bernard D.,Goodship Judith A.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference32 articles.

1. NKX2.5 mutations in patients with tetralogy of fallot;E Goldmuntz;Circulation,2001

2. Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations;JT Granados-Riveron;Congenit Heart Dis,2012

3. Building the mammalian heart from two sources of myocardial cells;M Buckingham;Nat Rev Genet,2005

4. GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5;V Garg;Nature,2003

5. Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect;K Hirayama-Yamada;Am J Med Genet A,2005

Cited by 54 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. Variants in FOXC1 and FOXC2 identified in patients with conotruncal heart defects;Genomics;2024-05

2. Human Genetics of Tetralogy of Fallot and Double-Outlet Right Ventricle;Advances in Experimental Medicine and Biology;2024

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

4. Mutations in genes related to myocyte contraction and ventricular septum development in non-syndromic tetralogy of Fallot;Frontiers in Cardiovascular Medicine;2023-09-28

5. The phenotypic spectrum of terminal and subterminal 6p deletions based on a social media-derived cohort and literature review;Orphanet Journal of Rare Diseases;2023-03-24