A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy-Reference-Cited by-同舟云学术

A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy

Published:2020-04 Issue: Volume:141 Page:17-29
ISSN:0022-2828
Container-title:Journal of Molecular and Cellular Cardiology
language:en
Short-container-title:Journal of Molecular and Cellular Cardiology

Author:

Brodehl Andreas,Weiss Jürgen,Debus Jana Davina,Stanasiuk Caroline,Klauke Bärbel,Deutsch Marcus André,Fox Henrik,Bax Jördis,Ebbinghaus Hans,Gärtner Anna,Tiesmeier Jens,Laser Thorsten,Peterschröder Andreas,Gerull Brenda,Gummert Jan,Paluszkiewicz Lech,Milting Hendrik

Funder

German Heart Foundation

University Bielefeld

Deutsche Forschungsgemeinschaft

Erich and Hanna Klessmann Foundation

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Molecular Biology

Reference46 articles.

1. Genetics of and pathogenic mechanisms in arrhythmogenic right ventricular cardiomyopathy;Vimalanathan;Biophys. Rev.,2018

2. Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy;Gerull;Nat. Genet.,2004