A Novel Dominant Mutation in Plakoglobin Causes Arrhythmogenic Right Ventricular Cardiomyopathy
- 1 November 2007
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 81 (5) , 964-973
- https://doi.org/10.1086/521633
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Mutant Desmocollin-2 Causes Arrhythmogenic Right Ventricular CardiomyopathyAmerican Journal of Human Genetics, 2006
- Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Associated with Mutations in the Desmosomal Gene Desmocollin-2American Journal of Human Genetics, 2006
- Suppression of canonical Wnt/ -catenin signaling by nuclear plakoglobin recapitulates phenotype of arrhythmogenic right ventricular cardiomyopathyJournal of Clinical Investigation, 2006
- Loss of desmoplakin isoform I causes early onset cardiomyopathy and heart failure in a Naxos-like syndromeJournal of Medical Genetics, 2005
- Remodeling of myocyte gap junctions in arrhythmogenic right ventricular cardiomyopathy due to a deletion in plakoglobin (Naxos disease)Published by Elsevier ,2004
- Plakoglobin Is O-Glycosylated Close to the N-terminal Destruction BoxPublished by Elsevier ,2003
- Desmosomal Cadherin Binding Domains of PlakoglobinPublished by Elsevier ,1996
- The binding of plakoglobin to desmosomal cadherins: patterns of binding sites and topogenic potential.The Journal of cell biology, 1996
- Identification of Plakoglobin Domains Required for Association with N-cadherin and α-CateninPublished by Elsevier ,1995
- Right Ventricular Cardiomyopathy and Sudden Death in Young PeopleNew England Journal of Medicine, 1988