The Locus of a Novel Gene Responsible for Arrhythmogenic Right-Ventricular Dysplasia Characterized by Early Onset and High Penetrance Maps to Chromosome 10p12-p14
- 1 January 2000
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 66 (1) , 148-156
- https://doi.org/10.1086/302713
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Arrhythmogenic Right Ventricular DysplasiaAnnual Review of Medicine, 1999
- Is Arrhythmogenic Right Ventricular Dysplasia, Uhlʼs Anomaly, and Right Ventricular Outflow Tract Tachycardia a Spectrum of the Same Disease?Cardiology in Review, 1997
- Sudden unexpected nontraumatic death in 54 young adults: A 30-year population-based studyThe American Journal of Cardiology, 1995
- The gene for arrhythmogenic right ventricular cardiomyopathy maps to chromosome 14q23–q24Human Molecular Genetics, 1994
- Sudden Death in Childhood Due to Right Ventricular Dysplasia: Report of Two CasesPediatric Pathology, 1994
- Overexpression of the vimentin gene in transgenic mice inhibits normal lens cell differentiation.The Journal of cell biology, 1989
- A polymorphic form of familial arrhythmogenic right ventricular dysplasiaThe American Journal of Cardiology, 1987
- Right ventricular dysplasia: a report of 24 adult cases.Circulation, 1982
- Arrhythmogenic right ventricular dysplasia: A cause of ventricular tachycardia in children with apparently normal heartsAmerican Heart Journal, 1981
- Inexcitable right ventricle and bilateral bundle branch block in Uhl's disease.Circulation, 1978