Association Between Genetic Variation in the <i>SCN10A</i> Gene and Cardiac Conduction Abnormalities in Patients With Hypertrophic Cardiomyopathy-Reference-Cited by-同舟云学术

Association Between Genetic Variation in the SCN10A Gene and Cardiac Conduction Abnormalities in Patients With Hypertrophic Cardiomyopathy

Published:2015 Issue:4 Volume:56 Page:421-427
ISSN:1349-2365
Container-title:International Heart Journal
language:en
Short-container-title:Int. Heart J.

Author:

Iio Chiharuko¹,Ogimoto Akiyoshi¹²,Nagai Takayuki¹,Suzuki Jun¹,Inoue Katsuji¹,Nishimura Kazuhisa¹,Uetani Teruyoshi¹,Okayama Hideki¹,Okura Takafumi¹,Shigematsu Yuji¹,Tabara Yasuharu³⁴,Kohara Katsuhiko³,Miki Tetsuro³,Hamada Mareomi⁵,Higaki Jitsuo¹

Affiliation:

1. Department of Cardiology, Pulmonology, Hypertension & Nephrology, Ehime University Graduate School of Medicine

2. Cardiovascular Division, Department of Medicine, Brigham and Women’s Hospital and Harvard Medical School

3. Department of Geriatric Medicine, Ehime University Graduate School of Medicine

4. Center for Genomic Medicine, Kyoto University Graduate School of Medicine

5. Department of Cardiology, Uwajima City Hospital

Publisher

International Heart Journal (Japanese Heart Journal)

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Reference36 articles.

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

3. 3. Otsuka H, Arimura T, Abe T, et al. Prevalence and distribution of sarcomeric gene mutations in Japanese patients with familial hypertrophic cardiomyopathy. Circ J 2012; 76: 453-61.

4. 4. Kubo T, Kitaoka H, Okawa M, et al. Genetic screening and double mutation in Japanese patients with hypertrophic cardiomyopathy. Circ J 2011; 75: 2654-9.

5. 5. Ogimoto A, Okayama H, Nagai T, et al. Impact of synergistic polymorphisms in adrenergic receptor-related genes and cardiovascular events in patients with dilated cardiomyopathy. Circ J 2012; 76: 2003-8.

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