Mitochondrial DNA mutations in the pathogenesis of human disease

Molecular Medicine Today

Volumn 6, Issue 11, 2000, Pages 425-432

  Chinnery, Patrick F ^a   Turnbull, Douglas M ^a  

^a NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIOXIDANT; DICHLOROACETIC ACID; MITOCHONDRIAL DNA; THIAMINE; UBIQUINONE; VITAMIN;

ANIMAL MODEL; DIET SUPPLEMENTATION; DISEASE TRANSMISSION; ENZYME DEFICIENCY; EXERCISE; GENE MUTATION; HEREDITARY OPTIC ATROPHY; HUMAN; KEARNS SAYRE SYNDROME; LACTIC ACIDOSIS; LEIGH DISEASE; MELAS SYNDROME; MITOCHONDRIAL MYOPATHY; MOUSE; MYOCLONUS EPILEPSY; MYOPATHY; NONHUMAN; PEARSON SYNDROME; PHENOTYPE; REVIEW;

ANIMALS; DISEASE MODELS, ANIMAL; DNA, MITOCHONDRIAL; EXTRACHROMOSOMAL INHERITANCE; HUMANS; INTERNET; MICE; MITOCHONDRIAL ENCEPHALOMYOPATHIES; MUTATION; PHENOTYPE;

ANIMALIA;

EID: 0033761979     PISSN: 13574310     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1357-4310(00)01805-0     Document Type: Review

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