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Journal Abstract Search

511 related items for PubMed ID: 32991883

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  • 3. 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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  • 7. Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.
    Jiang P, Liang M, Zhang C, Zhao X, He Q, Cui L, Liu X, Sun YH, Fu Q, Ji Y, Bai Y, Huang T, Guan MX.
    Hum Mol Genet; 2016 Aug 15; 25(16):3613-3625. PubMed ID: 27427386
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  • 9. Mitochondrial tRNAThr 15891C>G mutation was not associated with Leber's hereditary optic neuropathy in Han Chinese patients.
    Jiang Z, Yu J, Xia B, Zhuo G.
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016 Aug 15; 27(2):1564-6. PubMed ID: 25186221
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  • 14. Oxidative Stress Profile in Genetically Confirmed Cases of Leber's Hereditary Optic Neuropathy.
    Rovcanin B, Jancic J, Pajic J, Rovcanin M, Samardzic J, Djuric V, Nikolic B, Ivancevic N, Novakovic I, Kostic V.
    J Mol Neurosci; 2021 May 15; 71(5):1070-1081. PubMed ID: 33095398
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  • 18. Mitochondrial tRNA(Thr) A15951G mutation may not be associated with Leber's Hereditary Optic Neuropathy.
    Zhang X, Yu S, Tu Y, Huang W.
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016 Jul 15; 27(4):2323-5. PubMed ID: 26000946
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