Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep05616.pdf
Reference44 articles.
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3. Tomaselli, G. F. & Zipes, D. P. What causes sudden death in heart failure? Circ Res 95, 754–63 (2004).
4. Wang, Q. et al. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell 80, 805–11 (1995).
5. Chen, Q. et al. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature 392, 293–6 (1998).
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