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Journal Abstract Search

342 related items for PubMed ID: 17406640

  • 1. Epidemiology and penetrance of Leber hereditary optic neuropathy in Finland.
    Puomila A, Hämäläinen P, Kivioja S, Savontaus ML, Koivumäki S, Huoponen K, Nikoskelainen E.
    Eur J Hum Genet; 2007 Oct; 15(10):1079-89. PubMed ID: 17406640
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  • 5. X-Inactivation patterns in females harboring mtDNA mutations that cause Leber hereditary optic neuropathy.
    Hudson G, Carelli V, Horvath R, Zeviani M, Smeets HJ, Chinnery PF.
    Mol Vis; 2007 Dec 21; 13():2339-43. PubMed ID: 18199976
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  • 6. 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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  • 7. Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco-alcohol amblyopia.
    Korkiamäki P, Kervinen M, Karjalainen K, Majamaa K, Uusimaa J, Remes AM.
    Acta Ophthalmol; 2013 Nov 18; 91(7):630-4. PubMed ID: 22970697
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  • 11. Confirmation of the mitochondrial ND1 gene mutation G3635A as a primary LHON mutation.
    Yang J, Zhu Y, Tong Y, Chen L, Liu L, Zhang Z, Wang X, Huang D, Qiu W, Zhuang S, Ma X.
    Biochem Biophys Res Commun; 2009 Aug 14; 386(1):50-4. PubMed ID: 19497304
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  • 12. Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathy.
    Ventura DF, Gualtieri M, Oliveira AG, Costa MF, Quiros P, Sadun F, de Negri AM, Salomão SR, Berezovsky A, Sherman J, Sadun AA, Carelli V.
    Invest Ophthalmol Vis Sci; 2007 May 14; 48(5):2362-70. PubMed ID: 17460303
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  • 14. Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.
    Tharaphan P, Chuenkongkaew WL, Luangtrakool K, Sanpachudayan T, Suktitipat B, Suphavilai R, Srisawat C, Sura T, Lertrit P.
    J Neuroophthalmol; 2006 Dec 14; 26(4):264-7. PubMed ID: 17204919
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  • 18. Mitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese.
    Zhang AM, Zou Y, Guo X, Jia X, Zhang Q, Yao YG.
    Biochem Biophys Res Commun; 2009 Aug 21; 386(2):392-5. PubMed ID: 19527690
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