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. - Lopes LR; Macken WL; Preez SD; Kotwal H; Savvatis K; Sekhri N; Mohiddin SA; Kabiljo R; Pitceathly RDS (Human genomics, 2024)