Sodium channel mutations and arrhythmias
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
http://www.nature.com/articles/nrcardio.2009.44.pdf
Reference81 articles.
1. Wang, Q. et al. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell 80, 805–811 (1995).
2. Inherited Arrhythmias Database. [online January 2000] http://www.fsm.it/cardmoc/ (accessed 25 February 2009).
3. Chen, Q. et al. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nat. 392, 293–296 (1998).
4. Schott, J. J. et al. Cardiac conduction defects associate with mutations in SCN5A. Nature Genet. 23, 20–21 (1999).
5. Benson, D. W. et al. Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A). J. Clin. Invest. 112, 1019–1028 (2003).
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