Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity. (2021)
Attributed to:
The genetic aetiology of hypertropic cardiomyopathy
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41588-020-00764-0
PubMed Identifier: 33495597
Publication URI: http://europepmc.org/abstract/MED/33495597
Type: Journal Article/Review
Volume: 53
Parent Publication: Nature genetics
Issue: 2
ISSN: 1061-4036