Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients-Reference-Cited by-同舟云学术

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Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients

Published:2015 Issue:4 Volume:56 Page:450-453
ISSN:1349-2365
Container-title:International Heart Journal
language:en
Short-container-title:Int. Heart J.

Author:

Chang Ya-Sian¹²,Yang Yi-Wen²,Lin Yen-Nien³,Lin Kuo-Hung³,Chang Kuan-Cheng³⁴,Chang Jan-Gowth¹²⁴

Affiliation:

1. Epigenome Research Center, China Medical University Hospital

2. Department of Laboratory Medicine, China Medical University Hospital

3. Division of Cardiology, Department of Internal Medicine, China Medical University Hospital

4. School of Medicine, China Medical University

Publisher

International Heart Journal (Japanese Heart Journal)

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Reference30 articles.

1. 1. Bokil NJ, Baisden JM, Radford DJ, Summers KM. Molecular genetics of long QT syndrome. Mol Genet Metab 2010; 101: 1-8. (Review)

2. 2. Schwartz PJ, Stramba-Badiale M, Crotti L, et al. Prevalence of the congenital long-QT syndrome. Circulation 2009; 120: 1761-7.

3. 3. Kapplinger JD, Tester DJ, Salisbury BA, et al. Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test. Heart Rhythm 2009; 6: 1297-303.

4. 4. Tester DJ, Ackerman MJ. Genetics of long QT syndrome. Methodist Debakey Cardiovasc J 2014; 10: 29-33. (Review)

5. 5. Napolitano C, Priori SG, Schwartz PJ, et al. Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice. JAMA 2005; 294: 2975-80.

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