Loss-of-function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype. (2019)

First Author: Maruthappu T

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1111/bjd.17388

PubMed Identifier: 30382575

Publication URI: http://europepmc.org/abstract/MED/30382575

Type: Journal Article/Review

Volume: 180

Parent Publication: The British journal of dermatology

Issue: 5

ISSN: 0007-0963