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Journal Abstract Search

256 related items for PubMed ID: 19783880

  • 1. [Haplotype analysis and possible founder effect at the R778L mutation of the ATP7B gene in Korean patients with Wilson's disease].
    Bae SH, Kim JW, Seo JK.
    Korean J Hepatol; 2009 Sep; 15(3):309-19. PubMed ID: 19783880
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  • 3. [Haplotype analysis at R778L mutation of ATP7B gene in Korean patients with Wilson disease].
    Jin HS, Oh B.
    Korean J Hepatol; 2009 Sep; 15(3):295-8. PubMed ID: 19783878
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  • 7. [Wilson disease: an update].
    Seo JK.
    Korean J Hepatol; 2006 Sep; 12(3):333-63. PubMed ID: 16998287
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  • 8. Analysis and application of ATP7B gene mutations in 35 patients with hepatolenticular degeneration.
    Zong YN, Kong XD.
    Genet Mol Res; 2015 Dec 29; 14(4):18764-70. PubMed ID: 26782526
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  • 9. Common mutations of ATP7B in Wilson disease patients from Hungary.
    Firneisz G, Lakatos PL, Szalay F, Polli C, Glant TT, Ferenci P.
    Am J Med Genet; 2002 Feb 15; 108(1):23-8. PubMed ID: 11857545
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  • 10. p.H1069Q mutation in ATP7B and biochemical parameters of copper metabolism and clinical manifestation of Wilson's disease.
    Gromadzka G, Schmidt HH, Genschel J, Bochow B, Rodo M, Tarnacka B, Litwin T, Chabik G, Członkowska A.
    Mov Disord; 2006 Feb 15; 21(2):245-8. PubMed ID: 16211609
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  • 12. Direct sequencing of mutations in the copper-transporting P-type adenosine triphosphate (ATP7B) gene for diagnosis and pathogenesis of Wilson's disease.
    Zhang DF, Teng JF.
    Genet Mol Res; 2016 Sep 23; 15(3):. PubMed ID: 27706781
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  • 14. Distinct clinical courses according to presenting phenotypes and their correlations to ATP7B mutations in a large Wilson's disease cohort.
    Lee BH, Kim JH, Lee SY, Jin HY, Kim KJ, Lee JJ, Park JY, Kim GH, Choi JH, Kim KM, Yoo HW.
    Liver Int; 2011 Jul 23; 31(6):831-9. PubMed ID: 21645214
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  • 15. Clinical and genetic characterization of a large cohort of patients with Wilson's disease in China.
    Zhang S, Yang W, Li X, Pei P, Dong T, Yang Y, Zhang J.
    Transl Neurodegener; 2022 Feb 28; 11(1):13. PubMed ID: 35220961
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  • 19. [Mutation analysis of 35 Wilson's disease pedigrees].
    Zong Y, Kong X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Feb 28; 33(1):30-3. PubMed ID: 26829729
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