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HeartRhythm Case Reports
(Jul 2015)
Short QT and atrial fibrillation: A KCNQ1 mutation–specific disease. Late follow-up in three unrelated children
Georgia Sarquella-Brugada, MD,
Oscar Campuzano, PhD,
Anna Iglesias, MSc,
Josefina Grueso, MD, PhD,
David J. Bradley, MD,
Gunter Kerst, MD, PhD,
Daniel Shmorhun, MD, PhD,
Josep Brugada, MD, PhD,
Ramon Brugada, MD, PhD
Affiliations
Georgia Sarquella-Brugada, MD
Pediatric Arrhythmia Unit, Cardiology Service, Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain
Oscar Campuzano, PhD
Cardiovascular Genetics Center, University of Girona-IDIBGI, Girona, Spain
Anna Iglesias, MSc
Cardiovascular Genetics Center, University of Girona-IDIBGI, Girona, Spain
Josefina Grueso, MD, PhD
Hospital Virgen del Rocío, Universidad de Sevilla, Sevilla, Spain
David J. Bradley, MD
Section of Cardiology, Department of Pediatrics, MOTT Children’s Hospital, University of Michigan, Ann Arbor, Michigan
Gunter Kerst, MD, PhD
Pediatric Cardiology Department, University of Tuebingen, Tuebingen, Germany
Daniel Shmorhun, MD, PhD
Pediatric Electrophysiology Service, Walter Reed National Military Medical Center, Bethesda, Maryland
Josep Brugada, MD, PhD
Pediatric Arrhythmia Unit, Cardiology Service, Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain
Ramon Brugada, MD, PhD
Cardiovascular Genetics Center, University of Girona-IDIBGI, Girona, Spain
DOI
https://doi.org/10.1016/j.hrcr.2015.02.005
Journal volume & issue
Vol. 1, no. 4
pp. 193 – 197
Abstract
Read online
No abstracts available.
Keywords
Arrhythmia
Genetics
Pediatrics
Sudden death
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