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

American Journal of Human Genetics

Volumn 63, Issue 1, 1998, Pages 29-36

  Hanna, M G ^a   Nelson, I P ^a   Rahman, S ^b,c   Lane, R J M ^d   Land, J ^b   Heales, S ^b   Cooper, M J ^b   Schapira, A H V ^a,b   Morgan Hughes, J A ^a   Wood, N W ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b ROYAL FREE HOSPITAL   (United Kingdom)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d CHARING CROSS HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA;

ADULT; ARTICLE; CASE REPORT; DISEASE ASSOCIATION; DNA DEGRADATION; ENZYME DEFICIENCY; FEMALE; GENETIC ASSOCIATION; HUMAN; HUMAN CELL; HUMAN TISSUE; MUSCLE BIOPSY; POINT MUTATION; PRIORITY JOURNAL; STOP CODON;

POMACANTHUS MACULOSUS;

EID: 0032231458     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/301910     Document Type: Article

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