References
- Baklouti-Gargouri S, Ghorbel M, Ben Mahmoud A, Mkaouar-Rebai E, Cherif M, Chakroun N, Sellami A, et al. (2013). Mitochondrial DNA mutations and polymorphisms in asthenospermic infertile men. Mol Biol Rep 40:4705–12
- Boulet L, Karpati G, Shoubridge EA. (1992). Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF). Am J Hum Genet 51:1187–200
- Chinnery PF, Zwijnenburg PJ, Walker M, Howell N, Taylor RW, Lightowlers RN, Bindoff L, Turnbull DM. (1999). Nonrandom tissue distribution of mutant mtDNA. Am J Med Genet 85:498–501
- DiMauro S, Schon EA. (2001). Mitochondrial DNA mutations in human disease. Am J Med Genet 106:18–26
- Ding Y, Li Y, You J, Yang L, Chen B, Lu J, Guan MX. (2009). Mitochondrial tRNA(Glu) A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family. J Genet Genomics 36:241–50
- Güney AI, Javadova D, Kırac D, Ulucan K, Koc G, Ergec D, Tavukcu H, Tarcan T. (2012). Detection of Y chromosome microdeletions and mitochondrial DNA mutations in male infertility patients. Genet Mol Res 11:1039–48
- Reddy PL, Shetty VT, Dutt D, York A, Dar S, Mundle SD, Allampallam K, et al. (2002). Increased incidence of mitochondrial cytochrome c-oxidase gene mutations in patients with myelodysplastic syndromes. Br J Haematol 116:564–75
- Salas A, Yao YG, Macaulay V, Vega A, Carracedo A, Bandelt HJ. (2005). A critical reassessment of the role of mitochondria in tumorigenesis. PLoS Med 2:e296
- Spiropoulos J, Turnbull DM, Chinnery PF. (2002). Can mitochondrial DNA mutations cause sperm dysfunction? Mol Hum Reprod 8:719–21
- Stewart JB, Freyer C, Elson JL, Larsson NG. (2008). Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease. Nat Rev Genet 9:657–62
- Wallace DC. (2005). A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine. Annu Rev Genet 39:359–407
- Wallace DC, Stugard C, Murdock D, Schurr T, Brown MD. (1997). Ancient mtDNA sequences in the human nuclear genome: A potential source of errors in identifying pathogenic mutations. Proc Natl Acad Sci USA 94:14900–5
- Woischnik M, Moraes CT. (2002). Pattern of organization of human mitochondrial pseudogenes in the nuclear genome. Genome Res 12:885–93
- Yao YG, Kong QP, Salas A, Bandelt HJ. (2008). Pseudomitochondrial genome haunts disease studies. J Med Genet 45:769–72