The p.(Cys150Tyr) variant in CSRP3 is associated with late-onset hypertrophic cardiomyopathy in heterozygous individuals. (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/10.1016/j.ejmg.2020.104079
PubMed Identifier: 33035702
Publication URI: http://europepmc.org/abstract/MED/33035702
Type: Journal Article/Review
Volume: 63
Parent Publication: European journal of medical genetics
Issue: 12
ISSN: 1769-7212