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Journal Abstract Search

368 related items for PubMed ID: 33858285

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  • 22. Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients.
    Zhang AM, Jia X, Guo X, Zhang Q, Yao YG.
    J Transl Med; 2012 Mar 09; 10():43. PubMed ID: 22400981
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  • 25. 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 09; 98(6):826-31. PubMed ID: 24568867
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  • 26. Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy.
    Jiang P, Liang M, Zhang J, Gao Y, He Z, Yu H, Zhao F, Ji Y, Liu X, Zhang M, Fu Q, Tong Y, Sun Y, Zhou X, Huang T, Qu J, Guan MX.
    Invest Ophthalmol Vis Sci; 2015 Jul 09; 56(8):4778-88. PubMed ID: 26218905
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  • 27. Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy.
    Liang M, Jiang P, Li F, Zhang J, Ji Y, He Y, Xu M, Zhu J, Meng X, Zhao F, Tong Y, Liu X, Sun Y, Zhou X, Mo JQ, Qu J, Guan MX.
    Invest Ophthalmol Vis Sci; 2014 Mar 06; 55(3):1321-31. PubMed ID: 24398099
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  • 30. Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON).
    Peron C, Mauceri R, Cabassi T, Segnali A, Maresca A, Iannielli A, Rizzo A, Sciacca FL, Broccoli V, Carelli V, Tiranti V.
    Stem Cell Res; 2020 Oct 06; 48():101939. PubMed ID: 32771908
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  • 33. Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy.
    Achilli A, Iommarini L, Olivieri A, Pala M, Hooshiar Kashani B, Reynier P, La Morgia C, Valentino ML, Liguori R, Pizza F, Barboni P, Sadun F, De Negri AM, Zeviani M, Dollfus H, Moulignier A, Ducos G, Orssaud C, Bonneau D, Procaccio V, Leo-Kottler B, Fauser S, Wissinger B, Amati-Bonneau P, Torroni A, Carelli V.
    PLoS One; 2012 Oct 06; 7(8):e42242. PubMed ID: 22879922
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  • 34. Mitochondrial DNA variants in a cohort from Argentina with suspected Leber's hereditary optic neuropathy (LHON).
    Buonfiglio PI, Menazzi S, Francipane L, Lotersztein V, Ferreiro V, Elgoyhen AB, Dalamón V.
    PLoS One; 2023 Oct 06; 18(2):e0275703. PubMed ID: 36827238
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