Diseases of oxidative phosphorylation due to mtDNA mutations

Seminars in Neurology

Volumn 21, Issue 3, 2001, Pages 251-260

  DiMauro, S ^a   Andreu, A L ^a   Musumeci, O ^a   Bonilla, E ^a  

^a Columbia Univ Coll Physics Surg ^*  (United States)

Author keywords

Maternal inheritance; Mitochondria; Mitochondrial DNA (mtDNA); Mitochondrial encephalomyopathies; Respiratory chain

Indexed keywords

CELL NUCLEUS DNA; MITOCHONDRIAL DNA; PROTEIN;

CLINICAL FEATURE; ENCEPHALOMYOPATHY; EXERCISE; FAMILY HISTORY; GENE MUTATION; GENETIC REGULATION; HUMAN; LABORATORY; MOLECULAR GENETICS; MORPHOLOGY; MUSCLE; NEURORADIOLOGY; OXIDATIVE PHOSPHORYLATION; PRIORITY JOURNAL; RESPIRATORY CHAIN; REVIEW;

DNA, MITOCHONDRIAL; EDUCATION, MEDICAL, CONTINUING; HUMANS; MITOCHONDRIAL DISEASES; MUTATION;

EID: 0034770537     PISSN: 02718235     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2001-17942     Document Type: Review

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