Mitochondrial Genomics and Their Clinical Significance
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Publisher
Springer Nature Singapore
Link
https://link.springer.com/content/pdf/10.1007/978-981-97-3169-5_14
Reference119 articles.
1. Abdullah H, Shah S, Husain H, Hassan F, Maqsood H (2020) Late-onset mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome in a 63-year-old patient. Cureus 12(4):e7862. https://doi.org/10.7759/cureus.7862. PMID: 32483512; PMCID: PMC7255082
2. Al-Ghamdi BA, Al-Shamrani JM, El-Shehawi AM, Al-Johani I, Al-Otaibi BG (2022) Role of mitochondrial DNA in diabetes mellitus type I and type II. Saudi J Biol Sci 29(12):103434. https://doi.org/10.1016/j.sjbs.2022.103434. PMID: 36187456; PMCID: PMC9523097
3. AlSaman A, Tomoum H, Invernizzi F, Zeviani M (2012) Hepatocerebral form of mitochondrial DNA depletion syndrome due to mutation in MPV17 gene. Saudi J Gastroenterol 18:285–289
4. Anderson S, Bankier AT, Barrell BG, de Bruijn MH, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith AJ, Staden R, Young IG (1981) Sequence and organization of the human mitochondrial genome. Nature 290:457–465. [PubMed: 7219534]
5. Anderson S et al (1982) Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome. J Mol Biol 156:683–717
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