A molecular chaperone for mitochondrial complex I assembly is mutated in a progressive encephalopathy

Journal of Clinical Investigation

Volumn 115, Issue 10, 2005, Pages 2784-2792

  Ogilvie, Isla ^a   Kennaway, Nancy G ^b   Shoubridge, Eric A ^a,c  

^a MCGILL UNIVERSITY   (Canada)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^c MCGILL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CHAPERONE; HOLOENZYME; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE);

ARTICLE; CARDIOMYOPATHY; COMPLEX FORMATION; ENZYME DEFICIENCY; GENE MUTATION; HEART MITOCHONDRION; HUMAN; HUMAN CELL; LEIGH DISEASE; MITOCHONDRIAL MEMBRANE; NERVOUS SYSTEM FUNCTION; OXIDATIVE PHOSPHORYLATION; PHENOTYPE; PRIORITY JOURNAL; PROTEIN ASSEMBLY; RETROVIRUS; STRUCTURE ANALYSIS; VIRUS EXPRESSION;

BRAIN DISEASES, METABOLIC, INBORN; CELLS, CULTURED; CENTRAL NERVOUS SYSTEM; CHILD, PRESCHOOL; CODON, NONSENSE; ELECTRON TRANSPORT COMPLEX I; FEMALE; FIBROBLASTS; GENOME, HUMAN; HUMANS; MITOCHONDRIA; MOLECULAR CHAPERONES; OXIDATIVE PHOSPHORYLATION; RETROVIRIDAE; TRANSDUCTION, GENETIC;

EID: 26444488636     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI26020     Document Type: Article

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