APA (7th ed.) Citation

LR, L., WL, M., SD, P., H, K., K, S., N, S., . . . RDS, P. (2024). 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. Human genomics, 18(1), 136. https://doi.org/10.1186/s40246-024-00702-9

Chicago Style (17th ed.) Citation

LR, Lopes, Macken WL, Preez SD, Kotwal H, Savvatis K, Sekhri N, Mohiddin SA, Kabiljo R, and Pitceathly RDS. "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." Human Genomics 18, no. 1 (2024): 136. https://doi.org/10.1186/s40246-024-00702-9.

MLA (9th ed.) Citation

LR, Lopes, et al. "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." Human Genomics, vol. 18, no. 1, 2024, p. 136, https://doi.org/10.1186/s40246-024-00702-9.