📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

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