Specific Therapy Based on the Genotype in a Malignant Form of Long QT3, Carrying the V411M Mutation
Author:
Affiliation:
1. Inherited Arrhythmia Clinic
2. Division of Pacing and Electrophysiology, Rambam Health Care Campus, Technion Medical School
3. Department of Pediatric Cardiology, Rambam Health Care Campus and Bruce Rappaport Faculty of Medicine
Publisher
International Heart Journal (Japanese Heart Journal)
Subject
Cardiology and Cardiovascular Medicine,General Medicine
Link
https://www.jstage.jst.go.jp/article/ihj/60/4/60_18-705/_pdf
Reference25 articles.
1. 1. Moss AJ, Schwartz PJ, Crampton RS, et al. The long-QT syndrome: Prospective longitudinal study of 328 families. Circulation 1991; 84: 1136-44.
2. 2. Li K, Yang J, Guo W, et al. Video-assisted thoracoscopic left cardiac sympathetic denervation in Chinese patients with long QT syndrome. Int Heart J 2018; 59: 1346-51.
3. 3. Moss AJ. Management of patients with the hereditary long QT syndrome. J Cardiovasc Electrophysiol 1998; 9: 668-74.
4. 4. Schwartz PJ, Priori SG, Spazzolini C, et al. Genotype-phenotype in the long QT syndrome triggers for life threatening arrhythmia. Circulation 2001; 103: 89-95.
5. 5. Shimizu W, Aiba T, Antzelevitch C. Specific therapy based on the genotype and cellular mechanism in inherited cardiac arrhythmia. Long QT syndrome and Brugada syndrome. Curr Pharm Des 2005; 11: 1561-72.
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