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The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome
? TBD
scientific article published on June 2008
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Instance of
Scholarly article
Author
Lia Crotti
Peter J. Schwartz
Elijah Behr
Naoki Mochizuki
Dan Roden
Alfred L George
Subject
Phenotype
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