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Mitochondrial complex I deficiency in Parkinson's disease.
Schapira AH, Cooper JM, Dexter D, Clark JB, Jenner P, Marsden CD. Schapira AH, et al. Among authors: clark jb. J Neurochem. 1990 Mar;54(3):823-7. doi: 10.1111/j.1471-4159.1990.tb02325.x. J Neurochem. 1990. PMID: 2154550
Human mitochondrial respiratory chain deficiencies.
Morgan-Hughes JA, Schapira AH, Cooper JM, Hayes DJ, Clark JB. Morgan-Hughes JA, et al. Among authors: clark jb. Aust Paediatr J. 1988;24 Suppl 1:55-7. Aust Paediatr J. 1988. PMID: 2849394 Review.
Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype.
Morgan-Hughes JA, Sweeney MG, Cooper JM, Hammans SR, Brockington M, Schapira AH, Harding AE, Clark JB. Morgan-Hughes JA, et al. Among authors: clark jb. Biochim Biophys Acta. 1995 May 24;1271(1):135-40. doi: 10.1016/0925-4439(95)00020-5. Biochim Biophys Acta. 1995. PMID: 7599199 Free article.
469 results