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210 related items for PubMed ID: 10447650

  • 1. Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene.
    Besch D, Leo-Kottler B, Zrenner E, Wissinger B.
    Graefes Arch Clin Exp Ophthalmol; 1999 Sep; 237(9):745-52. PubMed ID: 10447650
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  • 2. 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; 5(4):233-40. PubMed ID: 8854108
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  • 3. [A case of Leber optic neuropathy with a new point mutation in the cytochrome b gene].
    Besch D, Wissinger B, Zrenner E, Leo-Kotter B.
    Ophthalmologe; 2000 Jan; 97(1):22-6. PubMed ID: 10663786
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  • 4. The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.
    Chinnery PF, Brown DT, Andrews RM, Singh-Kler R, Riordan-Eva P, Lindley J, Applegarth DA, Turnbull DM, Howell N.
    Brain; 2001 Jan; 124(Pt 1):209-18. PubMed ID: 11133798
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  • 5. A mutational hot spot in the mitochondrial ND6 gene in patients with Leber's hereditary optic neuropathy.
    Luberichs J, Leo-Kottler B, Besch D, Fauser S.
    Graefes Arch Clin Exp Ophthalmol; 2002 Feb; 240(2):96-100. PubMed ID: 11931086
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  • 6. 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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  • 7. Leber's hereditary optic neuropathy: clinical and molecular genetic results in a patient with a point mutation at np T11253C (isoleucine to threonine) in the ND4 gene and spontaneous recovery.
    Leo-Kottler B, Luberichs J, Besch D, Christ-Adler M, Fauser S.
    Graefes Arch Clin Exp Ophthalmol; 2002 Sep 19; 240(9):758-64. PubMed ID: 12271374
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  • 8. No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON.
    Gerbitz KD, Paprotta A, Obermaier-Kusser B, Rietschel M, Zerres K.
    FEBS Lett; 1992 Dec 21; 314(3):251-5. PubMed ID: 1361456
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  • 10. High incidence of visual recovery among four Japanese patients with Leber's hereditary optic neuropathy with the 14484 mutation.
    Yamada K, Mashima Y, Kigasawa K, Miyashita K, Wakakura M, Oguchi Y.
    J Neuroophthalmol; 1997 Jun 21; 17(2):103-7. PubMed ID: 9176781
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  • 11. Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutations.
    Nikoskelainen EK, Huoponen K, Juvonen V, Lamminen T, Nummelin K, Savontaus ML.
    Ophthalmology; 1996 Mar 21; 103(3):504-14. PubMed ID: 8600429
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  • 14. Confirmation of the 14568 mutation in the mitochondrial ND6 gene as causative in Leber's hereditary optic neuropathy.
    Fauser S, Leo-Kottler B, Besch D, Luberichs J.
    Ophthalmic Genet; 2002 Sep 21; 23(3):191-7. PubMed ID: 12324878
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  • 15. Leber's hereditary optic neuropathy.
    Letchavanakul A, Dechphongsaphilas W, Dhamcharee V.
    J Med Assoc Thai; 1999 Oct 21; 82(10):1051-5. PubMed ID: 10561972
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  • 18. Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy.
    Carelli V, Ghelli A, Bucchi L, Montagna P, De Negri A, Leuzzi V, Carducci C, Lenaz G, Lugaresi E, Degli Esposti M.
    Ann Neurol; 1999 Mar 21; 45(3):320-8. PubMed ID: 10072046
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  • 19. [Correlation between clinical and molecular genetic findings in Leber's optic atrophy].
    Leo-Kottler B, Christ-Adler M, Reck B, Wissinger B, Zrenner E.
    Ophthalmologe; 1995 Feb 21; 92(1):86-92. PubMed ID: 7719084
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  • 20. [Mitochondrial DNA mutation in Leber's hereditary optic neuropathy in China].
    Zhang LS, Huang Y, Li FY.
    Zhonghua Yi Xue Za Zhi; 1994 Jun 21; 74(6):349-51, 390. PubMed ID: 7994643
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