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Journal Abstract Search

279 related items for PubMed ID: 1900003

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  • 4. An example of Leber hereditary optic neuropathy not involving a mutation in the mitochondrial ND4 gene.
    Howell N, McCullough D.
    Am J Hum Genet; 1990 Oct; 47(4):629-34. PubMed ID: 2121024
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  • 5. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis.
    Kellar-Wood H, Robertson N, Govan GG, Compston DA, Harding AE.
    Ann Neurol; 1994 Jul; 36(1):109-12. PubMed ID: 8024249
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  • 8. Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathy.
    Vilkki J, Savontaus ML, Kalimo H, Nikoskelainen EK.
    Hum Genet; 1989 Jun; 82(3):208-12. PubMed ID: 2567271
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  • 9. Epidemic neuropathy in Cuba not associated with mitochondrial DNA mutations found in Leber's hereditary optic neuropathy patients. Cuba Neuropathy Field Investigation Team.
    Newman NJ, Torroni A, Brown MD, Lott MT, Fernandez MM, Wallace DC.
    Am J Ophthalmol; 1994 Aug 15; 118(2):158-68. PubMed ID: 8053461
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  • 10. [Molecular genetic analysis for Leber's hereditary optic neuropathy (LHON)].
    Tanno Y, Yoneda M, Tanaka K, Tsuji S.
    Nihon Rinsho; 1993 Sep 15; 51(9):2396-402. PubMed ID: 8411719
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  • 11. 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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  • 14. Leber's hereditary optic neuropathy. Clinical manifestations of the 3460 mutation.
    Johns DR, Smith KH, Miller NR.
    Arch Ophthalmol; 1992 Nov 18; 110(11):1577-81. PubMed ID: 1444915
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  • 15. Cytochrome c oxidase mutations in Leber hereditary optic neuropathy.
    Johns DR, Neufeld MJ.
    Biochem Biophys Res Commun; 1993 Oct 29; 196(2):810-5. PubMed ID: 8240356
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  • 16. Mutation detection in Leber's hereditary optic neuropathy by PCR with allele-specific priming.
    Nørby S, Lestienne P, Nelson I, Rosenberg T.
    Biochem Biophys Res Commun; 1991 Mar 15; 175(2):631-6. PubMed ID: 2018507
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  • 18. Screening for the two most frequent mutations in Leber's hereditary optic neuropathy by duplex PCR based on allele-specific amplification.
    Nørby S.
    Hum Mutat; 1993 Mar 15; 2(4):309-13. PubMed ID: 8401538
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  • 20. Mae III positively detects the mitochondrial mutation associated with type I Leber's hereditary optic neuropathy.
    Stone EM, Coppinger JM, Kardon RH, Donelson J.
    Arch Ophthalmol; 1990 Oct 15; 108(10):1417-20. PubMed ID: 1977373
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