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Journal Abstract Search

159 related items for PubMed ID: 16380132

  • 1. Leber's hereditary optic neuropathy with dystonia in a Japanese family.
    Watanabe M, Mita S, Takita T, Goto Y, Uchino M, Imamura S.
    J Neurol Sci; 2006 Apr 15; 243(1-2):31-4. PubMed ID: 16380132
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  • 2. Pediatric-onset dystonia associated with bilateral striatal necrosis and G14459A mutation in a Korean family: a case report.
    Kim IS, Ki CS, Park KJ.
    J Korean Med Sci; 2010 Jan 15; 25(1):180-4. PubMed ID: 20052369
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  • 3. 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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  • 8. 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. m.3635G>A mutation as a cause of Leber hereditary optic neuropathy.
    Kodroń A, Krawczyński MR, Tońska K, Bartnik E.
    J Clin Pathol; 2014 Jul 01; 67(7):639-41. PubMed ID: 24747208
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  • 10. Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation.
    Qu J, Zhou X, Zhang J, Zhao F, Sun YH, Tong Y, Wei QP, Cai W, Yang L, West CE, Guan MX.
    Ophthalmology; 2009 Mar 01; 116(3):558-564.e3. PubMed ID: 19167085
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  • 11. Leber's Hereditary Optic Neuropathy is Associated with Compound Primary Mutations of Mitochondrial ND1 m.3635G > A and ND6 m.14502 T > C.
    Jin X, Wang L, Gong Y, Chen B, Wang Y, Chen T, Wei S.
    Ophthalmic Genet; 2015 Mar 01; 36(4):291-8. PubMed ID: 24417559
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  • 13. Homoplasmy, heteroplasmy, and mitochondrial dystonia.
    McFarland R, Chinnery PF, Blakely EL, Schaefer AM, Morris AA, Foster SM, Tuppen HA, Ramesh V, Dorman PJ, Turnbull DM, Taylor RW.
    Neurology; 2007 Aug 28; 69(9):911-6. PubMed ID: 17724295
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  • 19. 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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  • 20. T14484C and T14502C in the mitochondrial ND6 gene are associated with Leber's hereditary optic neuropathy in a Chinese family.
    Zhang S, Wang L, Hao Y, Wang P, Hao P, Yin K, Wang QK, Liu M.
    Mitochondrion; 2008 Jun 03; 8(3):205-10. PubMed ID: 18440284
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