Human complex I defects in neurodegenerative diseases

Biochimica et Biophysica Acta - Bioenergetics

Volumn 1364, Issue 2, 1998, Pages 261-270

  Schapira, A H V ^a,b  

^a ROYAL FREE HOSPITAL   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Complex I; Dystonia; Leber's hereditary optic neuropathy; Mitochondrion; mtDNA; Parkinson's disease

Indexed keywords

DNA FRAGMENT; MITOCHONDRIAL DNA; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE);

APOPTOSIS; DEGENERATIVE DISEASE; DYSTONIA; ENZYME DEFICIENCY; GENE MUTATION; HEREDITARY OPTIC ATROPHY; HUMAN; MOUSE; NONHUMAN; PARKINSON DISEASE; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT; RESPIRATORY CHAIN; REVIEW;

EID: 0032490091     PISSN: 00052728     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0005-2728(98)00032-2     Document Type: Article

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