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205 related items for PubMed ID: 12736867

  • 1. Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy.
    Howell N, Oostra RJ, Bolhuis PA, Spruijt L, Clarke LA, Mackey DA, Preston G, Herrnstadt C.
    Am J Hum Genet; 2003 Jun; 72(6):1460-9. PubMed ID: 12736867
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  • 2. The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.
    Brown MD, Starikovskaya E, Derbeneva O, Hosseini S, Allen JC, Mikhailovskaya IE, Sukernik RI, Wallace DC.
    Hum Genet; 2002 Feb; 110(2):130-8. PubMed ID: 11935318
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  • 3. 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; 26(4):264-7. PubMed ID: 17204919
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  • 5. The epidemiology of Leber hereditary optic neuropathy in the North East of England.
    Yu-Wai-Man P, Griffiths PG, Brown DT, Howell N, Turnbull DM, Chinnery PF.
    Am J Hum Genet; 2003 Feb; 72(2):333-9. PubMed ID: 12518276
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  • 8. Leber's hereditary optic neuropathy--the spectrum of mitochondrial DNA mutations in Chinese patients.
    Yen MY, Wang AG, Chang WL, Hsu WM, Liu JH, Wei YH.
    Jpn J Ophthalmol; 2002 Feb; 46(1):45-51. PubMed ID: 11853713
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  • 10. Mitochondrial haplogroup background may influence Southeast Asian G11778A Leber hereditary optic neuropathy.
    Kaewsutthi S, Phasukkijwatana N, Joyjinda Y, Chuenkongkaew W, Kunhapan B, Tun AW, Suktitipat B, Lertrit P.
    Invest Ophthalmol Vis Sci; 2011 Jul 01; 52(7):4742-8. PubMed ID: 21398275
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  • 12. 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 01; 56(8):4778-88. PubMed ID: 26218905
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  • 13. 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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  • 14. Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees.
    Howell N, Kubacka I, Halvorson S, Howell B, McCullough DA, Mackey D.
    Genetics; 1995 May 01; 140(1):285-302. PubMed ID: 7635294
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  • 16. Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy.
    Khan NA, Govindaraj P, Jyothi V, Meena AK, Thangaraj K.
    Mol Vis; 2013 May 01; 19():1282-9. PubMed ID: 23805034
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  • 18. Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus.
    La Morgia C, Achilli A, Iommarini L, Barboni P, Pala M, Olivieri A, Zanna C, Vidoni S, Tonon C, Lodi R, Vetrugno R, Mostacci B, Liguori R, Carroccia R, Montagna P, Rugolo M, Torroni A, Carelli V.
    Neurology; 2008 Mar 04; 70(10):762-70. PubMed ID: 18216301
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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. Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation.
    Ji Y, Zhang AM, Jia X, Zhang YP, Xiao X, Li S, Guo X, Bandelt HJ, Zhang Q, Yao YG.
    Am J Hum Genet; 2008 Dec 03; 83(6):760-8. PubMed ID: 19026397
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