The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome
J. Clin. Invest. Naomasa Makita, et al.
doi:10.1172/JCI34057 [Go to this article.]

Problems with a PDF?

Copyright © 2008 by the American Society for Clinical Investigation.
Copying, redistribution, and other usage policies