Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block-Reference-Cited by-同舟云学术

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Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block

Published:2017-02-24 Issue:4 Volume:15 Page:2247-2254
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:en
Short-container-title:

Author:

Xu Ying-Jia,Qiu Xing-Biao,Yuan Fang,Shi Hong-Yu,Xu Lei,Hou Xu-Min,Qu Xin-Kai,Liu Xu,Huang Ri-Tai,Xue Song,Yang Yi-Qing,Li Ruo-Gu

Publisher

Spandidos Publications

Subject

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

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. NKX2.5 coding exons sequencing reveals novel non-synonymous mutations in patients with sporadic congenital heart diseases among the Tanzanian population;Egyptian Journal of Medical Human Genetics;2024-07-31

2. A Novel Missense Heterozygous Mutation in NKX2-5 Gene in a Family with Congenital Septal Defects and Cardiomyopathy: Case Series and Literature Review;Journal of Pediatric Genetics;2024-07-10

3. 2024 HRS expert consensus statement on arrhythmias in the athlete: Evaluation, treatment, and return to play;Heart Rhythm;2024-05

4. Unsupervised ensemble-based phenotyping enhances discoverability of genes related to left-ventricular morphology;Nature Machine Intelligence;2024-03-11

5. Atrial Septal Defects;Pediatric Cardiology;2024

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