Fingerprint
Dive into the research topics of 'The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
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 McKeown, Koji Miyamoto, Shiro Kamakura, Hiroyuki Tsutsui, Peter J. Schwartz, Alfred L. George, Dan M. Roden
Research output: Contribution to journal › Article › peer-review
188
Citations
(Scopus)