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5. Mitochondrial DNA deletions in muscle fibers in inclusion body myositis. Oldfors A; Moslemi AR; Fyhr IM; Holme E; Larsson NG; Lindberg C J Neuropathol Exp Neurol; 1995 Jul; 54(4):581-7. PubMed ID: 7602331 [TBL] [Abstract][Full Text] [Related]
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8. Characterization of the mitochondrial DNA abnormalities in the skeletal muscle of patients with inclusion body myositis. Horvath R; Fu K; Johns T; Genge A; Karpati G; Shoubridge EA J Neuropathol Exp Neurol; 1998 May; 57(5):396-403. PubMed ID: 9596410 [TBL] [Abstract][Full Text] [Related]
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13. Mitochondrial DNA deletions in inclusion body myositis. Oldfors A; Larsson NG; Lindberg C; Holme E Brain; 1993 Apr; 116 ( Pt 2)():325-36. PubMed ID: 8384916 [TBL] [Abstract][Full Text] [Related]
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20. Bcl-2, Bcl-x, and Bax expression by immunohistochemistry in inclusion body myositis: a study of 27 cases. Prayson RA; Yu AC Arch Pathol Lab Med; 2001 Oct; 125(10):1326-30. PubMed ID: 11570908 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]