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579 related items for PubMed ID: 16829155

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  • 4. Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.
    Sudoyo H, Suryadi H, Lertrit P, Pramoonjago P, Lyrawati D, Marzuki S.
    J Hum Genet; 2002; 47(11):594-604. PubMed ID: 12436196
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  • 5. Leber's hereditary optic neuroretinopathy (LHON) associated with mitochondrial DNA point mutation G11778A in two Croatian families.
    Martin-Kleiner I, Gabrilovac J, Bradvica M, Vidović T, Cerovski B, Fumić K, Boranić M.
    Coll Antropol; 2006 Mar; 30(1):171-4. PubMed ID: 16617593
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  • 7. [Sudden blindness: consider Leber's hereditary optic neuropathy].
    Schieving JH, de Vries BB, Hol F, Stroink H.
    Ned Tijdschr Geneeskd; 2008 Oct 25; 152(43):2313-6. PubMed ID: 19024058
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  • 9. Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation--A case report.
    Grazina MM, Diogo LM, Garcia PC, Silva ED, Garcia TD, Robalo CB, Oliveira CR.
    Eur J Paediatr Neurol; 2007 Mar 25; 11(2):115-8. PubMed ID: 17254817
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  • 10. White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation.
    Lev D, Yanoov-Sharav M, Watemberg N, Leshinsky-Silver E, Lerman-Sagie T.
    Eur J Paediatr Neurol; 2002 Mar 25; 6(2):121-3. PubMed ID: 11995959
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  • 14. Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathy.
    Ventura DF, Gualtieri M, Oliveira AG, Costa MF, Quiros P, Sadun F, de Negri AM, Salomão SR, Berezovsky A, Sherman J, Sadun AA, Carelli V.
    Invest Ophthalmol Vis Sci; 2007 May 25; 48(5):2362-70. PubMed ID: 17460303
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  • 15. Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis.
    Kim JY, Hwang JM, Park SS.
    Ann Neurol; 2002 May 25; 51(5):630-4. PubMed ID: 12112111
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  • 16. [Study on three common mitochondrial DNA mutations in Leber's hereditary optic neuropathy].
    Ma YX, Zhou YG, Zhang JP, Zhang QB, Liu WL, Ren CF, Li XY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Oct 25; 29(5):519-23. PubMed ID: 23042385
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  • 17. Leber's hereditary optic neuropathy mutations in ethambutol-induced optic neuropathy.
    Hwang JM, Kim J, Park SS.
    J Neurol; 2003 Jan 25; 250(1):87-9. PubMed ID: 12527998
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  • 18. Genetic analysis of Japanese pedigrees with Leber's hereditary optic neuropathy.
    Nakamura M.
    Kobe J Med Sci; 1993 Dec 25; 39(5-6):171-82. PubMed ID: 8182918
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  • 20. [Diagnostic and differential diagnostic potential of mitochondrial DNA assessment in patients with Leber's hereditary optic neuropathy].
    Feng X, Pu W, Gao D.
    Zhonghua Yan Ke Za Zhi; 2001 May 25; 37(3):174-7. PubMed ID: 11864415
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