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170 related items for PubMed ID: 15707996

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  • 6. Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation.
    Cai W, Fu Q, Zhou X, Qu J, Tong Y, Guan MX.
    J Genet Genomics; 2008 Nov; 35(11):649-55. PubMed ID: 19022198
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  • 9. Leber's hereditary optic neuropathy is associated with the mitochondrial ND6 T14484C mutation in three Chinese families.
    Sun YH, Wei QP, Zhou X, Qian Y, Zhou J, Lu F, Qu J, Guan MX.
    Biochem Biophys Res Commun; 2006 Aug 18; 347(1):221-5. PubMed ID: 16806060
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  • 10. Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families.
    Zhou X, Wei Q, Yang L, Tong Y, Zhao F, Lu C, Qian Y, Sun Y, Lu F, Qu J, Guan MX.
    Biochem Biophys Res Commun; 2006 Feb 03; 340(1):69-75. PubMed ID: 16364244
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  • 11. Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family.
    Qu J, Li R, Zhou X, Tong Y, Yang L, Chen J, Zhao F, Lu C, Qian Y, Lu F, Guan MX.
    Mitochondrion; 2007 Feb 03; 7(1-2):140-6. PubMed ID: 17300996
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  • 12. Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation.
    Tong Y, Sun YH, Zhou X, Zhao F, Mao Y, Wei QP, Yang L, Qu J, Guan MX.
    Mol Genet Metab; 2010 Apr 03; 99(4):417-24. PubMed ID: 20053576
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  • 20. Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India.
    Khan NA, Govindaraj P, Soumittra N, Sharma S, Srilekha S, Ambika S, Vanniarajan A, Meena AK, Uppin MS, Sundaram C, Bindu PS, Gayathri N, Taly AB, Thangaraj K.
    Invest Ophthalmol Vis Sci; 2017 Aug 01; 58(10):3923-3930. PubMed ID: 28768321
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