<i>MYH7</i> Gene-Related Mutation p.V878L Identified in a Chinese Family with Hypertrophic Cardiomyopathy-Reference-Cited by-同舟云学术

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MYH7 Gene-Related Mutation p.V878L Identified in a Chinese Family with Hypertrophic Cardiomyopathy

Published:2019-11-30 Issue:6 Volume:60 Page:1415-1420
ISSN:1349-2365
Container-title:International Heart Journal
language:en
Short-container-title:Int. Heart J.

Author:

Du Yuan¹,Wang Ya¹,Han Xiu¹,Feng Zhanbin²,Ma Aiqun¹³⁴

Affiliation:

1. Department of Cardiovascular Medicine, First Affiliated Hospital of Xi'an Jiaotong University

2. Department of Cardiovascular Medicine, Ninth Hospital of Xi'an

3. Shaanxi Key Laboratory of Molecular Cardiology, Xi'an Jiaotong University

4. Key Laboratory of Environment and Genes Related to Diseases, Xi'an Jiaotong University, Ministry of Education

Publisher

International Heart Journal (Japanese Heart Journal)

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

https://www.jstage.jst.go.jp/article/ihj/60/6/60_19-146/_pdf

Reference29 articles.

1. 1. Kittleson MD, Meurs KM, Harris SP. The genetic basis of hypertrophic cardiomyopathy in cats and humans. J Vet Cardiol 2015; 17: S53-73.

2. 2. Semsarian C, Ingles J, Maron MS, et al. New perspectives on the prevalence of hypertrophic cardiomyopathy. J Am Coll Cardiol 2015; 65: 1249-54.

3. 3. Zou Y, Song L, Wang Z, et al. Prevalence of idiopathic hypertrophic cardiomyopathy in China: a population-based echocardiographic analysis of 8080 adults. Am J Med 2004; 116: 14-8.

4. 4. Maron BJ, Maron MS. Hypertrophic cardiomyopathy. Lancet 2013; 381: 242-55.

5. 5. Pasipoularides A. Challenges and controversies in hypertrophic cardiomyopathy: clinical, genomic and basic science perspectives. Rev Esp Cardiol 2018; 71: 132-8.

Cited by 2 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. Mutation Analysis of MYH7 Gene Arg143Gln in Hypertrophic Cardiomyopathy;Advances in Clinical Medicine;2022

2. Bioinformatics analysis of differentially expressed genes in non alcoholic fatty liver disease using next generation sequencing data;2021-12-17

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