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Deletions of specific exons of FHOD3 detected by next-generation sequencing are associated with hypertrophic cardiomyopathy. (2020)

First Author: Ochoa JP

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/10.1111/cge.13759

PubMed Identifier: 32335906

Publication URI: http://europepmc.org/abstract/MED/32335906

Type: Journal Article/Review

Volume: 98

Parent Publication: Clinical genetics

Issue: 1

ISSN: 0009-9163