The Novel Desmin Variant p.Leu115Ile Is Associated With a Unique Form of Biventricular Arrhythmogenic Cardiomyopathy. (2021)

First Author: Protonotarios A
Attributed to:  Discovering the causes of mutation-negative hypertrophic cardiomyopathy funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.cjca.2020.11.017

PubMed Identifier: 33290826

Publication URI: http://europepmc.org/abstract/MED/33290826

Type: Journal Article/Review

Volume: 37

Parent Publication: The Canadian journal of cardiology

Issue: 6

ISSN: 0828-282X