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Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene |
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| Authors: | Merner Nancy D Hodgkinson Kathy A Haywood Annika F M Connors Sean French Vanessa M Drenckhahn Jörg-Detlef Kupprion Christine Ramadanova Kalina Thierfelder Ludwig McKenna William Gallagher Barry Morris-Larkin Lynn Bassett Anne S Parfrey Patrick S Young Terry-Lynn |
| Affiliation: | 1 Faculty of Medicine, Memorial University, St. John's, Newfoundland and Labrador A1B 3V6, Canada 2 Max-Delbrück Centrum für Molekulare Medizin, Max-Delbruck-Zentrum, Kostenstelle 1109, Robert-Roessle-Str 10, Berlin 13122, Germany 3 The Heart Hospital, 16-18 Westmoreland Street, London W1G 8PH, UK 4 Department of Pathology, James Paton Memorial Regional Health Centre, Gander, Newfoundland and Labrador A1V 1P7, Canada 5 Centre for Addiction and Mental Health, Clinical Genetics Research Program, University of Toronto, 1001 Queen Street West, Unit 4, Toronto, Ontario M6J 1H4, Canada |
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