Open AccessHomozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities
Author(s) -
Gianfranco Frigo,
Alessandra Rampazzo,
Barbara Bauce,
Kalliopi Pilichou,
Giorgia Beffagna,
Gian Antonio Danieli,
Andrea Nava,
Bortolo Martini
Publication year - 2007
Publication title -
ep europace
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.119
H-Index - 102
eISSN - 1532-2092
pISSN - 1099-5129
DOI - 10.1093/europace/eum053
Subject(s) - medicine , brugada syndrome , cardiology , ventricular tachycardia , electrocardiography
To describe a patient showing monomorphic ventricular tachycardia, ECG aspect of Brugada syndrome, and structural heart abnormalities due to a homozygous missense mutation in SCN5A.
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