The many clinical faces of cytochrome c oxidase deficiency

Advances in Experimental Medicine and Biology

Volumn 748, Issue , 2012, Pages 341-357

  Dimauro, Salvatore ^a   Tanji, Kurenai ^b   Schon, Eric A ^b  

^a College of Physicians and Surgeons ^*  (United States)

^b NewYork Presbyterian Hospital   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL NUCLEUS DNA; CYTOCHROME C OXIDASE; CYTOCHROME C OXIDASE I; CYTOCHROME C OXIDASE II; CYTOCHROME C OXIDASE III; MITOCHONDRIAL DNA; OXYGEN; SUCCINATE DEHYDROGENASE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CLINICAL FEATURE; COX GENE; CYTOCHROME C OXIDASE DEFICIENCY; DISEASE COURSE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ELECTRON TRANSPORT; ENZYME ACTIVITY; ENZYME REGULATION; ENZYME SUBUNIT; GENE; GENE DELETION; GENE MUTATION; HEART DISEASE; HETEROPLASMY; HISTOCHEMISTRY; HUMAN; KIDNEY DISEASE; LEIGH DISEASE; LIVER DISEASE; MITOCHONDRIAL RESPIRATION; MOLECULAR BIOLOGY; MUSCLE BIOPSY; NONHUMAN; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN PROTEIN INTERACTION; PROTON TRANSPORT; RESPIRATORY CHAIN;

CYTOCHROME-C OXIDASE DEFICIENCY; ELECTRON TRANSPORT COMPLEX IV; HUMANS; LEIGH DISEASE; MUTATION; PROTEIN SUBUNITS; SUCCINATE DEHYDROGENASE;

EID: 84863746788     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-4614-3573-0_14     Document Type: Article

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