Referenced in: none

Automatically associated channels: Kv7.1 , Nav1.5

Title: The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome.

Authors: Naomasa Makita, Elijah Behr, Wataru Shimizu, Minoru Horie, Akihiko Sunami, Lia Crotti, Eric Schulze-Bahr, Shigetomo Fukuhara, Naoki Mochizuki, Takeru Makiyama, Hideki Itoh, Michael Christiansen, Pascal McKeown, Koji Miyamoto, Shiro Kamakura, Hiroyuki Tsutsui, Peter J Schwartz, Alfred L George, Dan M Roden

Journal, date & volume: J. Clin. Invest., 2008 Jun , 118, 2219-29

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/18451998

Abstract