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An analysis of mitochondrial variation in cardiomyopathy patients from the 100,000 genomes cohort: m.4300A>G as a cause of genetically elusive hypertrophic cardiomyopathy. (2024)

First Author: Lopes LR

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/10.1186/s40246-024-00702-9

PubMed Identifier: 39639347

Publication URI: http://europepmc.org/abstract/MED/39639347

Type: Journal Article/Review

Volume: 18

Parent Publication: Human genomics

Issue: 1

ISSN: 1473-9542