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Journal Abstract Search

192 related items for PubMed ID: 18619472

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  • 2. Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation.
    Zhou X, Zhang H, Zhao F, Ji Y, Tong Y, Zhang J, Zhang Y, Yang L, Qian Y, Lu F, Qu J, Guan MX.
    Mol Genet Metab; 2010 Aug; 100(4):379-84. PubMed ID: 20627642
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  • 4. Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy.
    Qian Y, Zhou X, Hu Y, Tong Y, Li R, Lu F, Yang H, Mo JQ, Qu J, Guan MX.
    Biochem Biophys Res Commun; 2005 Jul 01; 332(2):614-21. PubMed ID: 15896721
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  • 9. Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese families.
    Qu J, Wang Y, Tong Y, Zhou X, Zhao F, Yang L, Zhang S, Zhang J, West CE, Guan MX.
    Invest Ophthalmol Vis Sci; 2010 Oct 01; 51(10):4906-12. PubMed ID: 20435583
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  • 10. [The analysis of Leber's hereditary optic neuropathy associated with mitochondrial tRNAAla C5601T mutation in seven Han Chinese families].
    Zhou HH, Dai XN, Lin B, Mi H, Liu XL, Zhao FX, Zhang JJ, Zhou XT, Sun YH, Wei QP, Qu J, Guan MX.
    Yi Chuan; 2012 Aug 01; 34(8):1031-42. PubMed ID: 22917908
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  • 12. Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.
    Tharaphan P, Chuenkongkaew WL, Luangtrakool K, Sanpachudayan T, Suktitipat B, Suphavilai R, Srisawat C, Sura T, Lertrit P.
    J Neuroophthalmol; 2006 Dec 01; 26(4):264-7. PubMed ID: 17204919
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  • 14. Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese families.
    Liu XL, Zhou X, Zhou J, Zhao F, Zhang J, Li C, Ji Y, Zhang Y, Wei QP, Sun YH, Yang L, Lin B, Yuan Y, Li Y, Qu J, Guan MX.
    Ophthalmology; 2011 May 01; 118(5):978-85. PubMed ID: 21131053
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  • 15. Two families with Leber's hereditary optic neuropathy carrying G11778A and T14502C mutations with haplogroup H2a2a1 in mitochondrial DNA.
    Qiao C, Wei T, Hu B, Peng C, Qiu X, Wei L, Yan M.
    Mol Med Rep; 2015 Aug 01; 12(2):3067-72. PubMed ID: 25936877
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  • 17. [Leber's hereditary optic neuropathy is associated with the mitochondrial G11696A mutation in two Chinese families].
    Zhao FX, Zhou XT, Qu J, Wei QP, Tong Y, Yang L, Lv JX, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Oct 01; 24(5):556-9. PubMed ID: 17922426
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  • 20. Low penetrance of the 14484 LHON mutation when it arises in a non-haplogroup J mtDNA background.
    Howell N, Herrnstadt C, Shults C, Mackey DA.
    Am J Med Genet A; 2003 Jun 01; 119A(2):147-51. PubMed ID: 12749053
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