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The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome
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 P. McKeown, Koji Miyamoto, Shiro Kamakura, Hiroyuki Tsutsui, Guy Schwartz, Alfred George, Dan Roden, Peter J. Schwartz
2008
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