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Journal Abstract Search

163 related items for PubMed ID: 7910006

  • 21. High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy.
    Mashima Y, Hiida Y, Oguchi Y, Kudoh J, Shimizu N.
    Hum Genet; 1993 Aug; 92(1):101-2. PubMed ID: 8103501
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  • 22. Leber's hereditary optic neuropathy.
    Letchavanakul A, Dechphongsaphilas W, Dhamcharee V.
    J Med Assoc Thai; 1999 Oct; 82(10):1051-5. PubMed ID: 10561972
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  • 25. [Diagnostic and differential diagnostic potential of mitochondrial DNA assessment in patients with Leber's hereditary optic neuropathy].
    Feng X, Pu W, Gao D.
    Zhonghua Yan Ke Za Zhi; 2001 May; 37(3):174-7. PubMed ID: 11864415
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  • 28. Genetic analysis of Japanese pedigrees with Leber's hereditary optic neuropathy.
    Nakamura M.
    Kobe J Med Sci; 1993 Dec; 39(5-6):171-82. PubMed ID: 8182918
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  • 29. [A molecular genetic study of Leber's disease].
    Zhang LS.
    Zhonghua Yan Ke Za Zhi; 1993 Mar; 29(2):103-4. PubMed ID: 8404350
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  • 30. Mae III positively detects the mitochondrial mutation associated with type I Leber's hereditary optic neuropathy.
    Stone EM, Coppinger JM, Kardon RH, Donelson J.
    Arch Ophthalmol; 1990 Oct; 108(10):1417-20. PubMed ID: 1977373
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  • 34. Sequence of mitochondrial DNA in patients with multiple sclerosis.
    Chalmers RM, Robertson N, DAS Compston, Harding AE.
    Ann Neurol; 1996 Aug; 40(2):239-43. PubMed ID: 8773606
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  • 35. [Positive diagnosis of Leber's hereditary optic neuropathy using molecular genetics].
    Souied E, Pisella PJ, Ossareh B, Brézin A, Junes P, Wild-Decrette C, Munnich A, Bonnefont JP, Mondon H.
    J Fr Ophtalmol; 1997 Aug; 20(1):65-70. PubMed ID: 9099286
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  • 36. Exclusive homoplasmic 11778 mutation in mitochondrial DNA of Chinese patients with Leber's hereditary optic neuropathy.
    Yen MY, Lee HC, Wang AG, Chang WL, Liu JH, Wei YH.
    Jpn J Ophthalmol; 1999 Aug; 43(3):196-200. PubMed ID: 10413253
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  • 37. White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation.
    Lev D, Yanoov-Sharav M, Watemberg N, Leshinsky-Silver E, Lerman-Sagie T.
    Eur J Paediatr Neurol; 2002 Aug; 6(2):121-3. PubMed ID: 11995959
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  • 38. Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathy.
    Vilkki J, Savontaus ML, Kalimo H, Nikoskelainen EK.
    Hum Genet; 1989 Jun; 82(3):208-12. PubMed ID: 2567271
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  • 39. Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy.
    Johns DR, Berman J.
    Biochem Biophys Res Commun; 1991 Feb 14; 174(3):1324-30. PubMed ID: 1900003
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  • 40. Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis.
    Kim JY, Hwang JM, Park SS.
    Ann Neurol; 2002 May 14; 51(5):630-4. PubMed ID: 12112111
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