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Journal Abstract Search

496 related items for PubMed ID: 17204919

  • 1. 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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  • 4. Haplogroup heterogeneity of LHON patients carrying the m.14484T>C mutation in India.
    Khan NA, Govindaraj P, Soumittra N, Srilekha S, Ambika S, Vanniarajan A, Meena AK, Uppin MS, Sundaram C, Taly AB, Bindu PS, Gayathri N, Thangaraj K.
    Invest Ophthalmol Vis Sci; 2013 Jun 10; 54(6):3999-4005. PubMed ID: 23674761
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  • 6. mtDNA haplogroup distribution in Chinese patients with Leber's hereditary optic neuropathy and G11778A mutation.
    Ji Y, Jia X, Zhang Q, Yao YG.
    Biochem Biophys Res Commun; 2007 Dec 14; 364(2):238-42. PubMed ID: 17942074
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  • 7. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
    Pénisson-Besnier I, Moreau C, Jacques C, Roger JC, Dubas F, Reynier P.
    Rev Neurol (Paris); 2001 May 14; 157(5):537-41. PubMed ID: 11438773
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  • 8. [Spectrum of pathogenic mtDNA mutations in Leber hereditary optic neuropathy families from Siberia].
    Volod'ko NV, L'vova MA, Starikovskaia EB, Derbeneva OA, Bychkov IIu, Mikhaĭlovskaia IE, Pogozheva IV, Fedotov FF, Soyan GV, Procaccio V, Wallace DC, Sukernik RI.
    Genetika; 2006 Jan 14; 42(1):89-97. PubMed ID: 16523671
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  • 9. [Rapid genetic screening of Leber's hereditary optic neuropathy with mtDNA G11778A mutation by AS-PCR with whole blood].
    Yang JH, Tong Y, Li BH, Chen YK.
    Zhonghua Yan Ke Za Zhi; 2005 Mar 14; 41(3):243-5. PubMed ID: 15840367
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  • 10. 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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  • 11. Mitochondrial abnormalities in patients with LHON-like optic neuropathies.
    Abu-Amero KK, Bosley TM.
    Invest Ophthalmol Vis Sci; 2006 Oct 21; 47(10):4211-20. PubMed ID: 17003408
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  • 12. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
    Mao YJ, Qu J, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb 21; 25(1):45-9. PubMed ID: 18247303
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  • 16. 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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  • 17. Reduced frequency of known mutations in a cohort of LHON patients from India.
    Sundaresan P, Kumar SM, Thompson S, Fingert JH.
    Ophthalmic Genet; 2010 Dec 01; 31(4):196-9. PubMed ID: 20809775
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  • 18. [Detection of mtDNA*LHON G11778A mutation by real-time polymerase chain reaction using TaqMan-MGB probe technology].
    Li YM, Wang JY, Chen Y, Shao JB, Wang J, Tong Y.
    Zhonghua Yan Ke Za Zhi; 2006 Aug 01; 42(8):728-32. PubMed ID: 17081446
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  • 20. Clinical, genetic, and biochemical characterization of a Leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations.
    Brown MD, Allen JC, Van Stavern GP, Newman NJ, Wallace DC.
    Am J Med Genet; 2001 Dec 15; 104(4):331-8. PubMed ID: 11754070
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