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Journal Abstract Search

71 related items for PubMed ID: 8320863

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  • 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
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  • 4. Identification of a novel T398A mutation in the ND5 subunit of the mitochondrial complex I and of three novel mtDNA polymorphisms in two patients presenting ocular symptoms.
    Batandier C, Picard A, Tessier N, Lunardi J.
    Hum Mutat; 2000 Dec 19; 16(6):532. PubMed ID: 11102991
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  • 7. 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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  • 12. Clinical spectrum of Leber's hereditary optic neuropathy.
    Kerrison JB, Newman NJ.
    Clin Neurosci; 1997 Oct 29; 4(5):295-301. PubMed ID: 9292259
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  • 14. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.
    Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM, Elsas LJ, Nikoskelainen EK.
    Science; 1988 Dec 09; 242(4884):1427-30. PubMed ID: 3201231
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  • 17. 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 Dec 09; 2(4):309-13. PubMed ID: 8401538
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  • 18. Identification and primary structure of five human NADH-ubiquinone oxidoreductase subunits.
    Ton C, Hwang DM, Dempsey AA, Liew CC.
    Biochem Biophys Res Commun; 1997 Dec 18; 241(2):589-94. PubMed ID: 9425316
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  • 20. Sequence of mitochondrial DNA in patients with multiple sclerosis.
    Chalmers RM, Robertson N, DAS Compston, Harding AE.
    Ann Neurol; 1996 Aug 18; 40(2):239-43. PubMed ID: 8773606
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