Intrinsic uncoupling of cytochrome c oxidase may cause the maternally inherited mitochondrial diseases MELAS and LHON

FEBS Letters

Volumn 433, Issue 1-2, 1998, Pages 93-97

  Mather, Michael W ^a   Rottenberg, Hagai ^a  

^a DREXEL UNIVERSITY COLLEGE OF MEDICINE   (United States)

Author keywords

Cytochrome c oxidase; Membrane potential; Mitochondrial disease; Paracoccus denitrificans; Proton pumping

Indexed keywords

CYTOCHROME C OXIDASE; PROTON PUMP;

ARTICLE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; GENE MUTATION; HEREDITARY OPTIC ATROPHY; MELAS SYNDROME; MEMBRANE POTENTIAL; NONHUMAN; PARACOCCUS DENITRIFICANS; PRIORITY JOURNAL;

ASCORBIC ACID; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX IV; GENE DELETION; GENE EXPRESSION; HUMANS; KINETICS; MELAS SYNDROME; ONIUM COMPOUNDS; OPTIC ATROPHIES, HEREDITARY; ORGANOPHOSPHORUS COMPOUNDS; PARACOCCUS DENITRIFICANS; PROTON PUMPS; TETRAMETHYLPHENYLENEDIAMINE;

EID: 0031812281     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-5793(98)00891-6     Document Type: Article

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