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Journal Abstract Search

174 related items for PubMed ID: 12749053

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  • 5. mtDNA haplogroup distribution in Chinese patients with Leber's hereditary optic neuropathy and G11778A mutation.
    Ji Y, Jia X, Zhang Q, Yao YG.
    Biochem Biophys Res Commun; 2007 Dec 14; 364(2):238-42. PubMed ID: 17942074
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  • 6. Strikingly different penetrance of LHON in two Chinese families with primary mutation G11778A is independent of mtDNA haplogroup background and secondary mutation G13708A.
    Wang HW, Jia X, Ji Y, Kong QP, Zhang Q, Yao YG, Zhang YP.
    Mutat Res; 2008 Aug 25; 643(1-2):48-53. PubMed ID: 18619472
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  • 8. Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy.
    Howell N, Oostra RJ, Bolhuis PA, Spruijt L, Clarke LA, Mackey DA, Preston G, Herrnstadt C.
    Am J Hum Genet; 2003 Jun 25; 72(6):1460-9. PubMed ID: 12736867
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  • 10. Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation.
    Qu J, Zhou X, Zhao F, Liu X, Zhang M, Sun YH, Liang M, Yuan M, Liu Q, Tong Y, Wei QP, Yang L, Guan MX.
    Biochim Biophys Acta; 2010 Mar 25; 1800(3):305-12. PubMed ID: 19733221
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  • 14. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
    Mao YJ, Qu J, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb 25; 25(1):45-9. PubMed ID: 18247303
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  • 16. 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 Feb 25; 47(11):594-604. PubMed ID: 12436196
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  • 18. Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background.
    Hudson G, Carelli V, Spruijt L, Gerards M, Mowbray C, Achilli A, Pyle A, Elson J, Howell N, La Morgia C, Valentino ML, Huoponen K, Savontaus ML, Nikoskelainen E, Sadun AA, Salomao SR, Belfort R, Griffiths P, Yu-Wai-Man P, de Coo RF, Horvath R, Zeviani M, Smeets HJ, Torroni A, Chinnery PF.
    Am J Hum Genet; 2007 Aug 25; 81(2):228-33. PubMed ID: 17668373
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  • 20. Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy.
    Dawod PGA, Jancic J, Marjanovic A, Brankovic M, Jankovic M, Samardzic J, Potkonjak D, Djuric V, Mesaros S, Novakovic I, Abdel Motaleb FI, Kostic VS, Nikolic D.
    Genes (Basel); 2020 Sep 02; 11(9):. PubMed ID: 32887465
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