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Myocardial Perfusion Defects in Hypertrophic Cardiomyopathy Mutation Carriers (2021)

First Author: Hughes R

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/10.1161/jaha.120.020227

PubMed Identifier: 34310159

Publication URI: http://europepmc.org/abstract/MED/34310159

Type: Journal Article/Review

Parent Publication: Journal of the American Heart Association

Issue: 15

ISSN: 2047-9980