Cryptic Splice-Altering Variants in MYBPC3 Are a Prevalent Cause of Hypertrophic Cardiomyopathy. (2020)
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/circgen.120.002905
PubMed Identifier: 32396390
Publication URI: http://europepmc.org/abstract/MED/32396390
Type: Journal Article/Review
Volume: 13
Parent Publication: Circulation. Genomic and precision medicine
Issue: 3
ISSN: 2574-8300