Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanisms by HOLT, I. J, HARDING, A. E, MORGAN-HUGHES, J. A

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Cytochrome c Oxidase Deficiency Associated with the First Stop-Codon Point Mutation in Human mtDNA by Hanna, M.G., Nelson, I.P., Rahman, S., Lane, R.J.M., Land, J., Heales, S., Cooper, M.J., Schapira, A.H.V., Morgan-Hughes, J.A., Wood, N.W.

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Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples by Hammans, S.R., Sweeney, M.G., Brockington, M., Morgan-Hughes, J.A., Harding, A.E.

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Mitochondrial encephalopathy with multiple mitochondrial DNA deletions: a report of two families and two sporadic cases with unusual clinical and neuropathological features by Chalmers, R.M, Brockington, M, Howard, R.S, Lecky, B.R.F, Morgan-Hughes, J.A, Harding, A.E

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Kearns-Sayre syndrome associated with mitochondrial DNA deletion or duplication: a molecular genetic and pathological study by Brockington, M., Alsanjari, N., Sweeney, M.G., Morgan-Hughes, J.A., Scaravilli, F., Harding, A.E.

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Fifty year follow-up of a patient with central core disease shows slow but definite progression by Lamont, P.J, Dubowitz, V, Landon, D.N, Davis, M, Morgan-Hughes, J.A

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Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A → G (MERRF) mutation: relationship to proportion of mutant mitochondrial D... by Hanna, M.G., Nelson, I.P., Morgan-Hughes, J.A., Harding, A.E.

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New phenotypic diversity associated with the mitochondrial tRNASer(UCN) gene mutation by Pulkes, T., Liolitsa, D., Eunson, L.H., Rose, M., Nelson, I.P., Rahman, S., Poulton, J., Marchington, D.R., Landon, D.N., Debono, A.G., Morgan-Hughes, J.A., Hanna, M.G.

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New phenotypic diversity associated with the mitochondrial tRNA Ser(UCN) gene mutation by Pulkes, T., Liolitsa, D., Eunson, L.H., Rose, M., Nelson, I.P., Rahman, S., Poulton, J., Marchington, D.R., Landon, D.N., Debono, A.G., Morgan-Hughes, J.A., Hanna, M.G.

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Erratum to “Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A → G (MERRF) mutation: relationship to proportion of mutant mit... by Hanna, M.G., Nelson, I.P., Morgan-Hughes, J.A., Harding, A.E.

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Erratum to “Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A → G (MERRF) mutation: relationship to proportion of mutant mit... by Hanna, M.G., Nelson, I.P., Morgan-Hughes, J.A., Harding, A.E.

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Cytochrome c oxidase deficiency linked to a new stop codon point mutation in mitochondrial DNA by Hanna, M.G., Nelson, I.P., Rahman, S., Schapira, A.H.V., Cooper, J.M., Morgan-Hughes, J.A., Wood, N.W.

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