The natural history of a genetic subtype of arrhythmogenic right ventricular cardiomyopathy caused by a p.S358L mutation in TMEM43

Author:

Hodgkinson KA,Connors SP1,Merner N2,Haywood A2,Young T-L2,McKenna WJ3,Gallagher B4,Curtis F2,Bassett AS5,Parfrey PS6

Affiliation:

1. Division of Cardiology; Memorial University; St. John's; Newfoundland; Canada

2. Discipline of Genetics; Memorial University, Health Sciences Centre; St. John's; Newfoundland; Canada

3. Institute of Cardiovascular Science; University College London and The Heart Hospital, University College London Hospitals Trust; London; UK

4. Division of Pathology; James Paton Memorial Hospital; Gander; Newfoundland; Canada

5. Clinical Genetics Research Program; Centre for Addiction & Mental Health, University of Toronto; Toronto; Ontario; Canada

6. Clinical Epidemiology Unit; Memorial University, Health Sciences Centre; St. John's; Newfoundland; Canada

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference30 articles.

1. Arrhythmogenic right ventricular cardiomyopathy;Ellinor;Heart Fail Clin,2010

2. Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia;Marcus;Eur Heart J,2010

3. http://www.hopkinsmedicine.org/heart_vascular_institute/clinical_services/arvd/_pdf/arvd_checklist_comparison.pdf Baltimore 2010

4. Total disconnection of right ventricular free wall: surgical treatment of right ventricular tachycardia associated with right ventricular dysplasia;Guiraudon;Circulation,1983

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