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2. Laser-excited fluorescence studies of mitochondrial function in saponin-skinned skeletal muscle fibers of patients with chronic progressive external ophthalmoplegia. Winkler K; Kuznetsov AV; Lins H; Kirches E; von Bossanyi P; Dietzmann K; Frank B; Feistner H; Kunz WS Biochim Biophys Acta; 1995 Dec; 1272(3):181-4. PubMed ID: 8541350 [TBL] [Abstract][Full Text] [Related]
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6. Multiple mitochondrial DNA deletions in a patient with mitochondrial myopathy and cardiomyopathy but no ophthalmoplegia. Takei Y; Ikeda S; Yanagisawa N; Takahashi W; Sekiguchi M; Hayashi T Muscle Nerve; 1995 Nov; 18(11):1321-5. PubMed ID: 7565930 [TBL] [Abstract][Full Text] [Related]
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13. A mitochondrial DNA duplication as a marker of skeletal muscle specific mutations in the mitochondrial genome. Mancuso M; Vives-Bauza C; Filosto M; Marti R; Solano A; Montoya J; Gamez J; DiMauro S; Andreu AL J Med Genet; 2004 Jun; 41(6):e73. PubMed ID: 15173239 [No Abstract] [Full Text] [Related]
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18. Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia. Moslemi AR; Melberg A; Holme E; Oldfors A Ann Neurol; 1996 Nov; 40(5):707-13. PubMed ID: 8957011 [TBL] [Abstract][Full Text] [Related]
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