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Page 1
Mitochondrial DNA polymerase-gamma and human disease.
Hudson G, Chinnery PF. Hudson G, et al. Among authors: chinnery pf. Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R244-52. doi: 10.1093/hmg/ddl233. Hum Mol Genet. 2006. PMID: 16987890 Review.
Treatment of mitochondrial disease.
Taylor RW, Chinnery PF, Clark KM, Lightowlers RN, Turnbull DM. Taylor RW, et al. Among authors: chinnery pf. J Bioenerg Biomembr. 1997 Apr;29(2):195-205. doi: 10.1023/a:1022646215643. J Bioenerg Biomembr. 1997. PMID: 9239544 Review.
Mitochondrial genotype and clinical phenotype.
Chinnery PF, Turnbull DM. Chinnery PF, et al. J Inherit Metab Dis. 1998 Jun;21(4):321-5. doi: 10.1023/a:1005357221101. J Inherit Metab Dis. 1998. PMID: 9700589 Review. No abstract available.
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: chinnery pf. Am J Hum Genet. 1999 May;64(5):1330-9. doi: 10.1086/302361. Am J Hum Genet. 1999. PMID: 10205264 Free PMC article.
Mitochondrial DNA and disease.
Chinnery PF, Turnbull DM. Chinnery PF, et al. Lancet. 1999 Jul;354 Suppl 1:SI17-21. doi: 10.1016/s0140-6736(99)90244-1. Lancet. 1999. PMID: 10437851 Review. No abstract available.
674 results