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181 related items for PubMed ID: 8240356

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathy.
    Wissinger B, Besch D, Baumann B, Fauser S, Christ-Adler M, Jurklies B, Zrenner E, Leo-Kottler B.
    Biochem Biophys Res Commun; 1997 May 19; 234(2):511-5. PubMed ID: 9177303
    [Abstract] [Full Text] [Related]

  • 3. Mitochondrial DNA mutations in Cuban optic and peripheral neuropathy.
    Johns DR, Neufeld MJ, Hedges TR.
    J Neuroophthalmol; 1994 Sep 19; 14(3):135-40. PubMed ID: 7804416
    [Abstract] [Full Text] [Related]

  • 4. 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 19; 38(4):693-700. PubMed ID: 8728098
    [Abstract] [Full Text] [Related]

  • 5. Cytochrome b mutations in Leber hereditary optic neuropathy.
    Johns DR, Neufeld MJ.
    Biochem Biophys Res Commun; 1991 Dec 31; 181(3):1358-64. PubMed ID: 1764087
    [Abstract] [Full Text] [Related]

  • 6. A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.
    Jun AS, Brown MD, Wallace DC.
    Proc Natl Acad Sci U S A; 1994 Jun 21; 91(13):6206-10. PubMed ID: 8016139
    [Abstract] [Full Text] [Related]

  • 7. A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I.
    Brown MD, Yang CC, Trounce I, Torroni A, Lott MT, Wallace DC.
    Am J Hum Genet; 1992 Aug 21; 51(2):378-85. PubMed ID: 1322638
    [Abstract] [Full Text] [Related]

  • 8. Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.
    Leo-Kottler B, Christ-Adler M, Baumann B, Zrenner E, Wissinger B.
    Ger J Ophthalmol; 1996 Jul 21; 5(4):233-40. PubMed ID: 8854108
    [Abstract] [Full Text] [Related]

  • 9. A patient with two mitochondrial DNA mutations causing PEO and LHON.
    Melberg A, Moslemi AR, Palm O, Raininko R, Stålberg E, Oldfors A.
    Eur J Med Genet; 2009 Jul 21; 52(1):47-8. PubMed ID: 19015050
    [Abstract] [Full Text] [Related]

  • 10. 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 Jul 21; 2(4):309-13. PubMed ID: 8401538
    [Abstract] [Full Text] [Related]

  • 11. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
    Pénisson-Besnier I, Moreau C, Jacques C, Roger JC, Dubas F, Reynier P.
    Rev Neurol (Paris); 2001 May 21; 157(5):537-41. PubMed ID: 11438773
    [Abstract] [Full Text] [Related]

  • 12. A family with Leber's hereditary optic neuropathy with mitochondrial 11778/ND4 and 4216/ND1 mutations.
    Hwang JM.
    Korean J Ophthalmol; 2000 Jun 21; 14(1):45-8. PubMed ID: 10933019
    [Abstract] [Full Text] [Related]

  • 13. Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy.
    Johns DR, Berman J.
    Biochem Biophys Res Commun; 1991 Feb 14; 174(3):1324-30. PubMed ID: 1900003
    [Abstract] [Full Text] [Related]

  • 14. Mitochondrial DNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nucleotide position 11,778.
    Matsumoto M, Hayasaka S, Hotta Y, Fujiki K, Fujimaki T, Takeda M, Ishida N, Endo S, Kanai A.
    J Hum Genet; 1998 Feb 14; 43(4):242-5. PubMed ID: 9852675
    [Abstract] [Full Text] [Related]

  • 15. Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.
    Brown MD, Voljavec AS, Lott MT, Torroni A, Yang CC, Wallace DC.
    Genetics; 1992 Jan 14; 130(1):163-73. PubMed ID: 1732158
    [Abstract] [Full Text] [Related]

  • 16. [Leber's hereditary optic neuropathy].
    Konrádová V, Zeman J, Stratilová L, Hermanská J, Vseticka I, Misovicová N, Kurca E, Gerinec A, Houstĕk J.
    Cas Lek Cesk; 1999 Oct 20; 138(18):565-8. PubMed ID: 10596473
    [Abstract] [Full Text] [Related]

  • 17. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes.
    Hofmann S, Bezold R, Jaksch M, Obermaier-Kusser B, Mertens S, Kaufhold P, Rabl W, Hecker W, Gerbitz KD.
    Genomics; 1997 Jan 01; 39(1):8-18. PubMed ID: 9027481
    [Abstract] [Full Text] [Related]

  • 18. [A molecular genetic study of Leber's disease].
    Zhang LS.
    Zhonghua Yan Ke Za Zhi; 1993 Mar 01; 29(2):103-4. PubMed ID: 8404350
    [Abstract] [Full Text] [Related]

  • 19. An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy.
    Johns DR, Neufeld MJ, Park RD.
    Biochem Biophys Res Commun; 1992 Sep 30; 187(3):1551-7. PubMed ID: 1417830
    [Abstract] [Full Text] [Related]

  • 20. [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 30; 44(7):676-80. PubMed ID: 8741498
    [Abstract] [Full Text] [Related]

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