Late-onset optic atrophy, ataxia, and myopathy associated with a mutation of a complex II gene

Annals of Neurology

Volumn 48, Issue 3, 2000, Pages 330-335

  Birch Machin, Mark A ^a   Taylor, Robert W ^a   Cochran, Bruce ^b   Ackrell, Brian A C ^b   Turnbull, Douglass M ^a  

^a NEWCASTLE UNIVERSITY   (United Kingdom)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CITRATE SYNTHASE; FLAVINE ADENINE NUCLEOTIDE; OXIDOREDUCTASE; SUCCINATE DEHYDROGENASE; SUCCINIC ACID; UBIQUINONE;

ALLELE; ARTICLE; ATAXIA; CLINICAL ARTICLE; DISEASE ASSOCIATION; ENZYME ACTIVITY; ENZYME BINDING; ENZYME INACTIVATION; ESCHERICHIA COLI; FEMALE; GENE MUTATION; GENETIC DISORDER; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; MYOPATHY; NEUROLOGIC DISEASE; OPTIC NERVE ATROPHY; PRIORITY JOURNAL; RESPIRATORY CHAIN;

AGE OF ONSET; ALLELES; ATAXIA; ELECTRON TRANSPORT COMPLEX II; HUMANS; MULTIENZYME COMPLEXES; MUSCULAR DISEASES; MUTATION; OPTIC ATROPHY; OXIDOREDUCTASES; PEDIGREE; SUCCINATE DEHYDROGENASE;

EID: 0033840193     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8249(200009)48:3<330::AID-ANA7>3.0.CO;2-A     Document Type: Article

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