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Cardiac myosin binding protein-C variants in paediatric-onset hypertrophic cardiomyopathy: natural history and clinical outcomes (2022)

First Author: Field E

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/10.1136/jmedgenet-2021-107774

PubMed Identifier: 34400558

Publication URI: http://europepmc.org/abstract/MED/34400558

Type: Journal Article/Review

Parent Publication: Journal of Medical Genetics

Issue: 8

ISSN: 0022-2593