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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 L

Attributed to: MitoCluster: an integrated phenotyping and mouse model generation platform for mitochondrial disease and dysfunction funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1186/s40246-024-00702-9

Publication URI: http://dx.doi.org/10.1186/s40246-024-00702-9

Type: Journal Article/Review

Parent Publication: Human Genomics

Issue: 1