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Journal Abstract Search

160 related items for PubMed ID: 8401538

  • 1. 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; 2(4):309-13. PubMed ID: 8401538
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  • 2. 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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  • 3. [Mitochondrial DNA mutation in Leber's hereditary optic neuropathy in China].
    Zhang LS, Huang Y, Li FY.
    Zhonghua Yi Xue Za Zhi; 1994 Jun; 74(6):349-51, 390. PubMed ID: 7994643
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  • 4. 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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  • 5. [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 15; 44(7):676-80. PubMed ID: 8741498
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  • 7. [Leber's optic neuropathy: new diagnostic prospects].
    Pagot V, Malecaze F, Rötig A, Simorre V, Maillard P, Mathis A, Munnich A.
    J Fr Ophtalmol; 1992 Jul 15; 15(1):19-23. PubMed ID: 1602101
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  • 8. A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies.
    Seibel P, Flierl A, Kottlors M, Reichmann H.
    Biochem Biophys Res Commun; 1994 Apr 29; 200(2):938-42. PubMed ID: 8179630
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  • 12. Clinical correlation of mitochondrial DNA heteroplasmy and Leber's hereditary optic neuropathy.
    Isashiki Y, Nakagawa M.
    Jpn J Ophthalmol; 1991 Apr 29; 35(3):259-67. PubMed ID: 1770665
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  • 15. 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 29; 5(4):233-40. PubMed ID: 8854108
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  • 16. Fast capillary electrophoresis-laser induced fluorescence analysis of ligase chain reaction products: human mitochondrial DNA point mutations causing Leber's hereditary optic neuropathy.
    Muth J, Williams PM, Williams SJ, Brown MD, Wallace DC, Karger BL.
    Electrophoresis; 1996 Dec 29; 17(12):1875-83. PubMed ID: 9034769
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  • 19. Mutation-specific PCR: a rapid and inexpensive diagnostic method, as exemplified by mitochondrial DNA analysis in Leber's hereditary optic neuropathy.
    Nørby S.
    DNA Cell Biol; 1993 Dec 29; 12(6):549-52. PubMed ID: 8101084
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