Congenital long QT syndrome (2008)
Crotti, Lia, Celano, Giuseppe, Dagradi, Federica, Schwartz, Peter J
Abstract Congenital long QT syndrome (LQTS) is a hereditary cardiac disease characterized by a prolongation of the QT interval at basal ECG and by a high risk of life-threatening arrhythmias. Disease...
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...
Crotti, Lia, Celano, Giuseppe, Dagradi, Federica, Schwartz, Peter J
Congenital long QT syndrome (LQTS) is a hereditary cardiac disease characterized by a prolongation of the QT interval at basal ECG and by a high risk of life-threatening arrhythmias. Disease...