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HeartRhythm Case Reports
(Sep 2015)
The lack of effect of sotalol in short QT syndrome patients carrying the T618I mutation in the KCNH2 gene
Carla Giustetto, MD,
Chiara Scrocco, MD,
Daniela Giachino, MD, PhD,
Claudio Rapezzi, MD,
Barbara Mognetti, PhD,
Fiorenzo Gaita, MD
Affiliations
Carla Giustetto, MD
Division of Cardiology, University of Torino, Department of Medical Sciences, Città della Salute e della Scienza Hospital, Torino, Italy
Chiara Scrocco, MD
Division of Cardiology, University of Torino, Department of Medical Sciences, Città della Salute e della Scienza Hospital, Torino, Italy
Daniela Giachino, MD, PhD
Medical Genetics, University of Torino, Department of Clinical and Biological Sciences, Torino, Italy
Claudio Rapezzi, MD
Institute of Cardiology, University of Bologna, and S. Orsola-Malpighi Hospital, Bologna, Italy
Barbara Mognetti, PhD
Pharmacology Unit, University of Torino, Department of Clinical and Biological Sciences, Torino, Italy
Fiorenzo Gaita, MD
Division of Cardiology, University of Torino, Department of Medical Sciences, Città della Salute e della Scienza Hospital, Torino, Italy
DOI
https://doi.org/10.1016/j.hrcr.2015.07.001
Journal volume & issue
Vol. 1, no. 5
pp. 373 – 378
Abstract
Read online
No abstracts available.
Keywords
Drug therapy
Genetics
Hydroquinidine
Polymorphisms
Short QT syndrome
Sotalol
Sudden death
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