Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6)

European Heart Journal - Tập 32 Số 9 - Trang 1077-1088 - 2011
Christian Templin1, Jelena R. Ghadri2, Jean‐Sébastien Rougier3, Alessandra Baumer4, Vladimir Kaplan2, Maxime Albesa3, Heinrich Sticht5, Anita Rauch4, Chris Puleo6, Dan Hu6, Héctor Barajas-Martínez6, Charles Antzelevitch6, Thomas F. Lüscher1,7, Hugues Abriel3, Fırat Duru1,8,7
1Cardiology, Cardiovascular Center, University Hospital Zurich, Raemistr. 100, 8091 Zurich, Switzerland
2Department of Internal Medicine, University Hospital Zurich, Zurich, Switzerland
3Department of Clinical Research, University of Bern, Murtenstr. 35, 3010 Bern, Switzerland
4Institute of Medical Genetics, University Hospital Zurich, Zurich, Switzerland
5Institute of Biochemistry, Friedrich-Alexander-University Erlangen-Nuernberg, Erlangen, Germany
6Masonic Medical Research Laboratory, Utica, NY, USA
7Zurich Center for Integrative Human Physiology (ZIHP), University Zurich, Zurich, Switzerland
8Division of Cardiac Arrhythmia and Electrophysiology, University Hospital Zurich, Zurich, Switzerland

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