Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.

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Published in Am J Hum Genet on July 01, 1998

Authors

M G Hanna1, I P Nelson, S Rahman, R J Lane, J Land, S Heales, M J Cooper, A H Schapira, J A Morgan-Hughes, N W Wood

Author Affiliations

1: Neurogenetics Section, University Department of Clinical Neurology, Institute of Neurology, London, WC1N 3BG, United Kingdom. mhanna@ion.ucl.ac.uk

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