The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome
Makita, Naomasa, Behr, Elijah, Shimizu, Wataru, Horie, Minoru, Sunami, Akihiko, Crotti, Lia, ...
Phenotypic overlap of type 3 long QT syndrome (LQT3) with Brugada syndrome (BrS) is observed in some carriers of mutations in the Na channel SCN5A. While this overlap is important for patient...