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6. Mitochondrial DNA Methylation and Related Disease. Gao D; Zhu B; Sun H; Wang X Adv Exp Med Biol; 2017; 1038():117-132. PubMed ID: 29178073 [TBL] [Abstract][Full Text] [Related]
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9. Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss. Kato T; Nishigaki Y; Noguchi Y; Ueno H; Hosoya H; Ito T; Kimura Y; Kitamura K; Tanaka M J Hum Genet; 2010 Mar; 55(3):147-54. PubMed ID: 20111055 [TBL] [Abstract][Full Text] [Related]
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14. Oxidative phosphorylation diseases. Disorders of two genomes. Shoffner JM; Wallace DC Adv Hum Genet; 1990; 19():267-330. PubMed ID: 2193491 [No Abstract] [Full Text] [Related]
15. Screening for aging-dependent point mutations in mtDNA. Michikawa Y; Attardi G Methods Mol Biol; 2002; 197():75-92. PubMed ID: 12013814 [No Abstract] [Full Text] [Related]
16. Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age. Corral-Debrinski M; Horton T; Lott MT; Shoffner JM; Beal MF; Wallace DC Nat Genet; 1992 Dec; 2(4):324-9. PubMed ID: 1303288 [TBL] [Abstract][Full Text] [Related]
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19. The transmission of OXPHOS disease and methods to prevent this. Jacobs LJ; de Wert G; Geraedts JP; de Coo IF; Smeets HJ Hum Reprod Update; 2006; 12(2):119-36. PubMed ID: 16199488 [TBL] [Abstract][Full Text] [Related]
20. A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies. Seibel P; Flierl A; Kottlors M; Reichmann H Biochem Biophys Res Commun; 1994 Apr; 200(2):938-42. PubMed ID: 8179630 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]