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The p.(Cys150Tyr) variant in CSRP3 is associated with late-onset hypertrophic cardiomyopathy in heterozygous individuals. (2020)

First Author: Salazar-Mendiguchía J

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