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Journal Abstract Search

169 related items for PubMed ID: 7981717

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  • 3. Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies.
    Liu CS, Cheng WL, Lee CF, Ma YS, Lin CY, Huang CC, Wei YH.
    Acta Neurol Scand; 2006 May; 113(5):334-41. PubMed ID: 16629770
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  • 4. Detection of known base substitution mutations in human mitochondrial DNA of MERRF and MELAS by biochip technology.
    Du W, Li W, Chen G, Cao H, Tang H, Tang X, Jin Q, Sun Z, Zhao H, Zhou W, He S, Lv Y, Zhao J, Zhang X.
    Biosens Bioelectron; 2009 Apr 15; 24(8):2371-6. PubMed ID: 19155171
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  • 5. [Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA].
    Stratilová L, Zeman J, Hansíková H, Houstĕk J, Hermanská J, Dudková Z, Konrádová V, Hůlková H, Elleder M.
    Cas Lek Cesk; 1998 Jul 13; 137(14):430-3. PubMed ID: 9748738
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  • 6. A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies.
    Seibel P, Flierl A, Kottlors M, Reichmann H.
    Biochem Biophys Res Commun; 1994 Apr 29; 200(2):938-42. PubMed ID: 8179630
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  • 7. A novel point mutation in the mitochondrial tRNA(Ser(UCN)) gene detected in a family with MERRF/MELAS overlap syndrome.
    Nakamura M, Nakano S, Goto Y, Ozawa M, Nagahama Y, Fukuyama H, Akiguchi I, Kaji R, Kimura J.
    Biochem Biophys Res Commun; 1995 Sep 05; 214(1):86-93. PubMed ID: 7669057
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  • 9. MELAS- and Kearns-Sayre-type co-mutation [corrected] with myopathy and autoimmune polyendocrinopathy.
    Ohno K, Yamamoto M, Engel AG, Harper CM, Roberts LR, Tan GH, Fatourechi V.
    Ann Neurol; 1996 Jun 05; 39(6):761-6. PubMed ID: 8651648
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  • 12. [Mitochondrial DNA mutations and three major forms of mitochondrial myopathies: CPEO, MELAS and MERRF].
    Goto Y.
    Nihon Rinsho; 1997 Dec 05; 55(12):3259-64. PubMed ID: 9436447
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  • 16. Mitochondrial cytopathies.
    Schmiedel J, Jackson S, Schäfer J, Reichmann H.
    J Neurol; 2003 Mar 05; 250(3):267-77. PubMed ID: 12638015
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  • 18. Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene.
    Akanuma J, Muraki K, Komaki H, Nonaka I, Goto Y.
    J Hum Genet; 2000 Mar 05; 45(6):337-41. PubMed ID: 11185741
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  • 19. [The correlation of the heteroplasmy of mtDNA and clinicopathological findings in the patients with mitochondrial encephalomyopathies].
    Tanno Y, Tanaka K, Tsuji S.
    Nihon Rinsho; 1997 Dec 05; 55(12):3270-6. PubMed ID: 9436449
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