Genetics of Mitochondrial Cardiomyopathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Pharmacology
Link
https://link.springer.com/content/pdf/10.1007/s12170-023-00715-4.pdf
Reference92 articles.
1. • Meyers DE, Basha HI, Koenig MK. Mitochondrial cardiomyopathy: pathophysiology, diagnosis, and management. Tex Heart Inst J. 2013;40(4):385–94. Excellent review of mitochondrial cardiomyopathies.
2. Lee SR, Kim N, Noh YH, et al. Mitochondrial DNA, mitochondrial dysfunction, and cardiac manifestations. Front Biosci (Landmark Ed). 2017;22(7):1177–94. https://doi.org/10.2741/4541.
3. Elorza AA, Soffia JP. mtDNA heteroplasmy at the core of aging-associated heart failure. An integrative view of OXPHOS and mitochondrial life cycle in cardiac mitochondrial physiology. Front Cell Dev Biol. 2021;9:625020. https://doi.org/10.3389/fcell.2021.625020.
4. • Bates MG, Bourke JP, Giordano C, d’Amati G, Turnbull DM, Taylor RW. Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management. Eur Heart J. 2012;33(24):3023–33. https://doi.org/10.1093/eurheartj/ehs275. Excellent review of mitochondrial cardiomyopathies.
5. Taylor RW, Giordano C, Davidson MM, et al. A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy. J Am Coll Cardiol. 2003;41(10):1786–96. https://doi.org/10.1016/s0735-1097(03)00300-0.
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