SCN5A Mutations Associated With Overlap Phenotype of Long QT Syndrome Type 3 and Brugada Syndrome
Author:
Affiliation:
1. Department of Pharmacology, Chiba University Graduate School of Medicine
Publisher
Japanese Circulation Society
Subject
Cardiology and Cardiovascular Medicine,General Medicine
Link
https://www.jstage.jst.go.jp/article/circj/78/5/78_CJ-14-0319/_pdf
Reference10 articles.
1. 1. Remme CA, Wilde AAM, Bezzina CR. Cardiac sodium channel overlap syndromes: Different faces of SCN5A mutations. Trend Cardiovasc Med 2008; 18: 78–87.
2. 2. Makita N. Phenotypic overlap of cardiac sodium channelopathies: Individual-specific or mutation-specific? Circ J 2009; 73: 810–817.
3. 3. Bezzina C, Veldkamp MW, van den Berg MP, Postma AV, Rook MB, Viersma J-W, et al. A single Na+ channel mutation causing both long-QT and Brugada syndromes. Circ Res 1999; 85: 1206–1213.
4. 4. Grant AO, Carboni MP, Neplioueva V, Starmer F, Memmi M, Napolitano C, et al. Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation. J Clin Invest 2002; 110: 1201–1209.
5. 5. Makita N, Behr E, Shimizu W, Horie M, Sunami A, Crotti L, et al. The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome. J Clin Invest 2008; 118: 2219–2229.
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