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Journal Abstract Search

163 related items for PubMed ID: 7910006

  • 1. Mitochondrial DNA mutations in Leber's optic neuropathy.
    Hurko O.
    Ann Neurol; 1994 May; 35(5):636. PubMed ID: 7910006
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  • 8. Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathy.
    Yoneda M, Tsuji S, Yamauchi T, Inuzuka T, Miyatake T, Horai S, Ozawa T.
    Lancet; 1989 May 13; 1(8646):1076-7. PubMed ID: 2566021
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  • 11. Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy.
    Holt IJ, Miller DH, Harding AE.
    J Neurol Neurosurg Psychiatry; 1988 Aug 13; 51(8):1075-7. PubMed ID: 2905730
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  • 12. [Analysis of mutations and heteroplasmy at mitochondrial DNA 11778 using non-RI single strand conformation polymorphisms in Leber's hereditary optic neuropathy].
    Toyo-Oka Y, Wada C, Yamabe H, Inoue M, Ishigaki M, Matsuyama N, Ohnuki Y, Ichibe Y, Wakakura M, Ohtani H.
    Rinsho Byori; 1996 Jul 13; 44(7):676-80. PubMed ID: 8741498
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  • 15. Mitochondrial DNA mutations associated with the 11778 mutation in Leber's disease.
    Sawano T, Tanaka M, Ohno K, Yoneda M, Ota Y, Terasaki H, Awaya S, Ozawa T.
    Biochem Mol Biol Int; 1996 Apr 13; 38(4):693-700. PubMed ID: 8728098
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  • 17. A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy.
    Singh G, Lott MT, Wallace DC.
    N Engl J Med; 1989 May 18; 320(20):1300-5. PubMed ID: 2566116
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  • 18. [Genetic basis of Leber's hereditary optic neuroretinopathy].
    Krawczyński MR, Pecold K.
    Klin Oczna; 1993 Jun 18; 95(6):219-22. PubMed ID: 8309190
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