Myocardial Perfusion Defects in Hypertrophic Cardiomyopathy Mutation Carriers. (2021)
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
Volume: 10
Parent Publication: Journal of the American Heart Association
Issue: 15
ISSN: 2047-9980