A Common Mutation of Long QT Syndrome Type 1 in Japan-Reference-Cited by-同舟云学术

A Common Mutation of Long QT Syndrome Type 1 in Japan

Published:2015 Issue:9 Volume:79 Page:2026-2030
ISSN:1346-9843
Container-title:Circulation Journal
language:en
Short-container-title:Circ J

Author:

Itoh Hideki¹²³,Dochi Kenichi¹,Shimizu Wataru⁴⁵,Denjoy Isabelle⁶,Ohno Seiko¹,Aiba Takeshi⁵,Kimura Hiromi¹,Kato Koichi¹,Fukuyama Megumi¹,Hasagawa Kanae¹,Schulze-Bahr Eric⁷⁸,Guicheney Pascale²³,Horie Minoru¹

Affiliation:

1. Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science

2. Sorbonne Universités, Institut de Recherche sur les Maladies Cardiovasculaires, du Métabolisme et de la Nutrition

3. Institute of Cardiometabolism and Nutrition (ICAN)

4. Division of Cardiology, Department of Internal Medicine, Nippon Medical School

5. Division of Arrhythmia and Electrophysiology, Department of Cardiovascular Medicine, National Cerebral and Cardiovascular Center

6. AP-HP, Hôpital Bichat, Service de Cardiologie, Centre de Référence des Maladies Cardiaques Héréditaires, Université Denis Diderot

7. Institute for Genetics of Heart Diseases (IfGH), Department of Cardiovascular Medicine, University Hospital Münster

8. Interdisciplinary Centre for Clinical Research (IZKF) of the University of Münster

Publisher

Japanese Circulation Society

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

https://www.jstage.jst.go.jp/article/circj/advpub/0/advpub_CJ-15-0342/_pdf

Reference26 articles.

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3. 3. Mizusawa Y, Horie M, Wilde AA. Genetic and clinical advances in congenital long QT syndrome. Circ J 2014; 78: 2827–2833.

4. 4. Schwartz PJ, Ackerman MJ, George AL, Wilde AA. Impact of genetics on the clinical management of channelopathies. J Am Coll Cardiol 2013; 62: 169–180.

5. 5. Wang Q, Curran ME, Splawski I, Burn TC, Millholland JM, VanRaay TJ, et al. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nat Genet 1996; 12: 17–23.

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