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Biochimica et Biophysica Acta - Bioenergetics

Volumn 1410, Issue 2, 1999, Pages 159-170

Mitochondrial involvement in Parkinson's disease, Huntington's disease, hereditary spastic paraplegia and Friedreich's ataxia

(1) Schapira, A H V a

a ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL (United Kingdom)

Author keywords

Hereditary spastic paraplegia; Huntington's disease; Mitochondrion; Parkinson's disease

Indexed keywords

ALPHA TOCOPHEROL; FRATAXIN; FREE RADICAL; IRON; MITOCHONDRIAL DNA; MITOCHONDRIAL ENZYME; MUTANT PROTEIN;

CLINICAL FEATURE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENVIRONMENT; FRIEDREICH ATAXIA; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUNTINGTON CHOREA; INHERITANCE; MITOCHONDRION; OXIDATIVE PHOSPHORYLATION; PARKINSON DISEASE; PATHOGENESIS; PRIORITY JOURNAL; REVIEW;

ANIMALS; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT; ENVIRONMENT; FRIEDREICH ATAXIA; HUMANS; HUNTINGTON DISEASE; IRON-BINDING PROTEINS; MITOCHONDRIA; NAD(P)H DEHYDROGENASE (QUINONE); PARKINSON DISEASE; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); SPASTIC PARAPLEGIA, HEREDITARY;

ATAXIA;

EID: 0033032999 PISSN: 00052728 EISSN: None Source Type: Journal
DOI: 10.1016/S0005-2728(98)00164-9 Document Type: Review

Times cited : (291)

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