TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome-Reference-Cited by-同舟云学术

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TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome

Published:2016-03-24 Issue:5 Volume:13 Page:4349-4356
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:en
Short-container-title:

Author:

GUO DONG-FENG,LI RUO-GU,YUAN FANG,SHI HONG-YU,HOU XU-MIN,QU XIN-KAI,XU YING-JIA,ZHANG MIN,LIU XU,JIANG JIN-QI,YANG YI-QING,QIU XING-BIAO

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Cited by 25 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. Atrial fibrillation variant-to-gene prioritization through cross-ancestry eQTL and single-nucleus multiomic analyses;iScience;2024-09

2. Investigating the role connective tissue fibroblasts play in the altered muscle anatomy associated with the limb abnormality, Radial Dysplasia;Journal of Anatomy;2024-04-16

3. TBX5 variants and cardiac phenotype: A systematic review of the literature and a novel variant;European Journal of Medical Genetics;2024-04

4. Nr2f1a maintains atrial nkx2.5 expression to repress pacemaker identity within venous atrial cardiomyocytes of zebrafish;eLife;2023-05-15

5. Genetics of sinoatrial node function and heart rate disorders;Disease Models & Mechanisms;2023-05-01

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