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SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism.
J Am Coll Cardiol. 2011 May 24;57(21):2160-8. doi: 10.1016/j.jacc.2010.09.084.
J Am Coll Cardiol. 2011.
PMID: 21596231
Free PMC article.
SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia.
McNair WP, Ku L, Taylor MR, Fain PR, Dao D, Wolfel E, Mestroni L; Familial Cardiomyopathy Registry Research Group.
McNair WP, et al.
Circulation. 2004 Oct 12;110(15):2163-7. doi: 10.1161/01.CIR.0000144458.58660.BB. Epub 2004 Oct 4.
Circulation. 2004.
PMID: 15466643
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