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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.
The molecular pathology of human respiratory chain defects.
Morgan-Hughes JA, Cooper JM, Schapira AH, Sweeny M, Holt IJ, Harding AE, Clark JB. Morgan-Hughes JA, et al. Among authors: clark jb. Rev Neurol (Paris). 1991;147(6-7):450-4. Rev Neurol (Paris). 1991. PMID: 1962049 Review.
Mitochondrial myopathies: genetic defects.
Harding AE, Holt IJ, Cooper JM, Schapira AH, Sweeney M, Clark JB, Morgan-Hughes JA. Harding AE, et al. Among authors: clark jb. Biochem Soc Trans. 1990 Aug;18(4):519-22. doi: 10.1042/bst0180519. Biochem Soc Trans. 1990. PMID: 2276422 Review. No abstract available.
Mitochondrial myopathies: clinical defects.
Morgan-Hughes JA, Cooper JM, Holt IJ, Harding AE, Schapira AH, Clark JB. Morgan-Hughes JA, et al. Among authors: clark jb. Biochem Soc Trans. 1990 Aug;18(4):523-6. doi: 10.1042/bst0180523. Biochem Soc Trans. 1990. PMID: 2276423 No abstract available.
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.
470 results