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Journal Abstract Search

211 related items for PubMed ID: 31817256

  • 1. Mitochondrial DNA Variation of Leber's Hereditary Optic Neuropathy in Western Siberia.
    Starikovskaya E, Shalaurova S, Dryomov S, Nazhmidenova A, Volodko N, Bychkov I, Mazunin I, Sukernik R.
    Cells; 2019 Dec 04; 8(12):. PubMed ID: 31817256
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  • 2. 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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  • 3. Pathogenic mitochondrial DNA mutations and associated clinical features in Korean patients with Leber's hereditary optic neuropathy.
    Yum HR, Chae H, Shin SY, Kim Y, Kim M, Park SH.
    Invest Ophthalmol Vis Sci; 2014 Oct 23; 55(12):8095-101. PubMed ID: 25342614
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  • 7. ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait.
    Behbehani R, Melhem M, Alghanim G, Behbehani K, Alsmadi O.
    Br J Ophthalmol; 2014 Jun 23; 98(6):826-31. PubMed ID: 24568867
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  • 10. mtDNA m.3635G>A may be classified as a common primary mutation for Leber hereditary optic neuropathy in the Chinese population.
    Jia X, Li S, Wang P, Guo X, Zhang Q.
    Biochem Biophys Res Commun; 2010 Dec 10; 403(2):237-41. PubMed ID: 21074518
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  • 11. Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C.
    Yu D, Jia X, Zhang AM, Li S, Zou Y, Zhang Q, Yao YG.
    PLoS One; 2010 Oct 18; 5(10):e13426. PubMed ID: 20976138
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  • 12. Leber's hereditary optic neuropathy (LHON) in an Apulian cohort of subjects.
    Bianco A, Bisceglia L, Trerotoli P, Russo L, D'Agruma L, Guerriero S, Petruzzella V.
    Acta Myol; 2017 Sep 18; 36(3):163-177. PubMed ID: 29774306
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  • 13. Mitochondrial Genetic Heterogeneity in Leber's Hereditary Optic Neuropathy: Original Study with Meta-Analysis.
    Jha RK, Dawar C, Hasan Q, Pujar A, Gupta G, Vishnu VY, Kekunnaya R, Thangaraj K.
    Genes (Basel); 2021 Aug 24; 12(9):. PubMed ID: 34573281
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  • 14. 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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