Influence of genetic modifiers on sudden cardiac death cases
Author:
Funder
Feith Foundation
Foundation Forensisches Forum
Publisher
Springer Science and Business Media LLC
Subject
Pathology and Forensic Medicine
Link
http://link.springer.com/article/10.1007/s00414-017-1739-7/fulltext.html
Reference36 articles.
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2. Schwartz PJ, Moss AJ, Vincent GM, Crampton RS (1993) Diagnostic criteria for the long QT syndrome. An update. Circulation 88(2):782–784. https://doi.org/10.1161/01.CIR.88.2.782
3. Mizusawa Y, Horie M, Am WA (2014) Genetic and clinical advances in congenital long QT syndrome. Circ J 78(12):2827–2833. https://doi.org/10.1253/circj.CJ-14-0905
4. Splawski I, Shen J, Timothy KW, Vincent GM, Lehmann MH, Keating MT (1998) Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1. Genomics 51(1):86–97. https://doi.org/10.1006/geno.1998.5361
5. Curran ME, Splawski I, Timothy KW, Vincen G, Green ED, Keating MTA (1995) Molecular basis for cardiac arrhythmia. HERG mutations cause long QT syndrome. Cell 80(5):795–803. https://doi.org/10.1016/0092-8674(95)90358-5
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