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Presence of an RYR2 Mutation is Associated with Sudden Cardiac Events at Presentation in Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)
Authors:J. Kozlovski  J. Ingles  V. Connell  L. Hunt  J. McGaughran  C. Turner  A. Davis  C. Semsarian
Affiliation:1. Sydney Medical School, The University of Sydney, Sydney, Australia;2. Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Sydney, Australia;3. Cardiology Department, The Royal Children''s Hospital, Parkville, Australia;4. Genetic Health Queensland, Royal Brisbane and Women''s Hospital, Brisbane, Australia;5. The Heart Centre for Children, The Children''s Hospital at Westmead, Sydney, Australia;1. Department of Internal Medicine, Cleveland Clinic, Cleveland, OH, 44195, USA;2. Section of Cardiovascular Imaging, Robert and Suzanne Tomsich Department of Cardiovascular Medicine, Sydell and Arnold Miller Family Heart, Vascular and Thoracic Institute, Cleveland Clinic, Cleveland, OH, 44195, USA;3. Section of Cardiovascular and Thoracic Radiology, Imaging Institute, Cleveland Clinic, Cleveland, OH, 44195, USA;1. Clinical Centre of Serbia, Cardiology Clinic, Belgrade, Serbia;2. Department of Cardiology, Charité-University-Medicine Berlin, Campus Virchow Klinikum, Berlin, Germany;1. Department of Cardiology, St. Michael''s Hospital, Toronto, Ontario, Canada;2. Department of Cardiology, Michael Garron Hospital, Toronto, Ontario, Canada;3. Department of Cardiology, Women''s College Hospital, Toronto, Ontario, Canada;4. Institut Universitaire de Cardiologie et de Pneumologie de Québec/Quebec Heart and Lung Institute, Québec City, Québec, Canada;5. Department of Cardiology, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada
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