Mitochondrial respiratory chain disorders II: Neurodegenerative disorders and nuclear gene defects

Lancet

Volumn 355, Issue 9201, 2000, Pages 389-394

  Leonard, J V ^a   Schapira, A H V ^b  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

FRATAXIN; HUNTINGTIN; MITOCHONDRIAL DNA; MITOCHONDRIAL ENZYME; NUCLEAR PROTEIN; RIBOSOME RNA; THYMIDINE PHOSPHORYLASE; TRANSFER RNA;

ALZHEIMER DISEASE; ANIMAL EXPERIMENT; ANIMAL MODEL; APOPTOSIS; DEGENERATIVE DISEASE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; EPILEPSY; FRIEDREICH ATAXIA; GENE MUTATION; GENETIC ANALYSIS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUNTINGTON CHOREA; LEIGH DISEASE; MITOCHONDRIAL MYOPATHY; NEUROPATHOLOGY; NONHUMAN; OXIDATIVE PHOSPHORYLATION; PARKINSON DISEASE; PRIORITY JOURNAL; PROTEIN DEFICIENCY; RESPIRATORY CHAIN; REVIEW; WILSON DISEASE;

EID: 0034728096     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(99)05226-5     Document Type: Review

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