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Reversal of a mitochondrial DNA defect in human skeletal muscle.
Clark KM, Bindoff LA, Lightowlers RN, Andrews RM, Griffiths PG, Johnson MA, Brierley EJ, Turnbull DM. Clark KM, et al. Among authors: johnson ma. Nat Genet. 1997 Jul;16(3):222-4. doi: 10.1038/ng0797-222. Nat Genet. 1997. PMID: 9207784 No abstract available.
Role of mitochondrial DNA mutations in disease and aging.
Cottrell DA, Blakely EL, Borthwick GM, Johnson MA, Taylor GA, Brierley EJ, Ince PG, Turnbull DM. Cottrell DA, et al. Among authors: johnson ma. Ann N Y Acad Sci. 2000 Jun;908:199-207. doi: 10.1111/j.1749-6632.2000.tb06647.x. Ann N Y Acad Sci. 2000. PMID: 10911959 Review.
An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy.
Clark KM, Taylor RW, Johnson MA, Chinnery PF, Chrzanowska-Lightowlers ZM, Andrews RM, Nelson IP, Wood NW, Lamont PJ, Hanna MG, Lightowlers RN, Turnbull DM. Clark KM, et al. Among authors: johnson ma. Am J Hum Genet. 1999 May;64(5):1330-9. doi: 10.1086/302361. Am J Hum Genet. 1999. PMID: 10205264 Free PMC article.
1,567 results