Characterization of the mitochondrial DNA abnormalities in the skeletal muscle of patients with inclusion body myositis

Journal of Neuropathology and Experimental Neurology

Volumn 57, Issue 5, 1998, Pages 396-403

  Horvath, Rita ^a   Fu, Katherine ^a   Johns, Timothy ^a   Genge, Angela ^a   Karpati, George ^a   Shoubridge, Eric A ^a,b  

^a MCGILL UNIVERSITY   (Canada)

^b MCGILL UNIVERSITY   (Canada)

Author keywords

Inclusion body myositis; Inflammatory myopathy; Mitochondrial DNA

Indexed keywords

CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA; SUCCINATE DEHYDROGENASE;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; FAMILIAL DISEASE; FEMALE; GENE DELETION; HUMAN; HUMAN TISSUE; IN SITU HYBRIDIZATION; INCLUSION BODY MYOSITIS; MALE; PRIORITY JOURNAL; SKELETAL MUSCLE;

EID: 0031808684     PISSN: 00223069     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005072-199805000-00003     Document Type: Article

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