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Journal Abstract Search

470 related items for PubMed ID: 8042948

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  • 2. The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study.
    Hammans SR, Sweeney MG, Hanna MG, Brockington M, Morgan-Hughes JA, Harding AE.
    Brain; 1995 Jun; 118 ( Pt 3)():721-34. PubMed ID: 7600089
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  • 8. Mitochondrial encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNALeu(UUR) gene.
    Shoffner JM, Bialer MG, Pavlakis SG, Lott M, Kaufman A, Dixon J, Teichberg S, Wallace DC.
    Neurology; 1995 Feb; 45(2):286-92. PubMed ID: 7854527
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  • 11. A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.
    Goto Y, Nonaka I, Horai S.
    Nature; 1990 Dec 13; 348(6302):651-3. PubMed ID: 2102678
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  • 12. A new point mutation at nucleotide pair 3291 of the mitochondrial tRNA(Leu(UUR)) gene in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Goto Y, Tsugane K, Tanabe Y, Nonaka I, Horai S.
    Biochem Biophys Res Commun; 1994 Aug 15; 202(3):1624-30. PubMed ID: 7520241
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  • 16. Defects of mitochondrial DNA.
    Zeviani M, Antozzi C.
    Brain Pathol; 1992 Apr 15; 2(2):121-32. PubMed ID: 1341953
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  • 17. Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patients.
    Börner GV, Zeviani M, Tiranti V, Carrara F, Hoffmann S, Gerbitz KD, Lochmüller H, Pongratz D, Klopstock T, Melberg A, Holme E, Pääbo S.
    Hum Mol Genet; 2000 Mar 01; 9(4):467-75. PubMed ID: 10699170
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  • 19. [MELAS (mitochondrial myopathy, encephalopathy lactic acidosis, and stroke-like episodes): clinical features and mitochondrial DNA mutations].
    Goto Y.
    Nihon Rinsho; 1993 Sep 01; 51(9):2373-8. PubMed ID: 8411715
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  • 20. Organ distribution of mutant mitochondrial tRNA(leu(UUR)) gene in a MELAS patient.
    Hamazaki S, Koshiba M, Sugiyama T.
    Acta Pathol Jpn; 1993 Apr 01; 43(4):187-91. PubMed ID: 8493868
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