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Journal Abstract Search

621 related items for PubMed ID: 26253413

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  • 3. Mutation spectrum and polymorphisms in ATP7B identified on direct sequencing of all exons in Chinese Han and Hui ethnic patients with Wilson's disease.
    Gu YH, Kodama H, Du SL, Gu QJ, Sun HJ, Ushijima H.
    Clin Genet; 2003 Dec; 64(6):479-84. PubMed ID: 14986826
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  • 5. A genetic study of Wilson's disease in the United Kingdom.
    Coffey AJ, Durkie M, Hague S, McLay K, Emmerson J, Lo C, Klaffke S, Joyce CJ, Dhawan A, Hadzic N, Mieli-Vergani G, Kirk R, Elizabeth Allen K, Nicholl D, Wong S, Griffiths W, Smithson S, Giffin N, Taha A, Connolly S, Gillett GT, Tanner S, Bonham J, Sharrack B, Palotie A, Rattray M, Dalton A, Bandmann O.
    Brain; 2013 May; 136(Pt 5):1476-87. PubMed ID: 23518715
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  • 7. Novel ATPase Cu(2+) transporting beta polypeptide mutations in Chinese families with Wilson's disease.
    Gu S, Yang H, Qi Y, Deng X, Zhang L, Guo Y, Huang Q, Li J, Shi X, Song Z, Deng H.
    PLoS One; 2013 May; 8(7):e66526. PubMed ID: 23843956
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  • 10. Spectrum and Classification of ATP7B Variants in a Large Cohort of Chinese Patients with Wilson's Disease Guides Genetic Diagnosis.
    Dong Y, Ni W, Chen WJ, Wan B, Zhao GX, Shi ZQ, Zhang Y, Wang N, Yu L, Xu JF, Wu ZY.
    Theranostics; 2016 May; 6(5):638-49. PubMed ID: 27022412
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  • 13. Screening for mutations in ATP7B gene using conformation-sensitive gel electrophoresis in a family with Wilson's disease.
    Sundaresan S, Eapen CE, Shaji RV, Chandy M, Kurian G, Chandy G.
    Med Sci Monit; 2007 Mar; 13(3):CS38-40. PubMed ID: 17325640
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  • 14. ATP7B mutations in families in a predominantly Southern Indian cohort of Wilson's disease patients.
    Santhosh S, Shaji RV, Eapen CE, Jayanthi V, Malathi S, Chandy M, Stanley M, Selvi S, Kurian G, Chandy GM.
    Indian J Gastroenterol; 2006 Mar; 25(6):277-82. PubMed ID: 17264425
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  • 15. Value of molecular analysis of Wilson's disease in the absence of tissue copper deposits: a novel ATP7B mutation in an adult patient.
    Kok KF, Hoevenaars B, Waanders E, Drenth JP.
    Neth J Med; 2008 Sep; 66(8):348-50. PubMed ID: 18809983
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  • 16. [Genotype-phenotype relationship and genetics study of 115 cases with Wilson's disease].
    Xia JK, Ning HF, Luo X, Zeng Y, Chen YB, Kong XD.
    Zhonghua Gan Zang Bing Za Zhi; 2024 Jun 20; 32(6):558-562. PubMed ID: 38964899
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  • 17. Mutation Analysis of the ATP7B Gene in Seven Chinese Families with Wilson's Disease.
    Xiao H, Deng S, Deng X, Gu S, Yang Z, Yin H, Deng H.
    Digestion; 2019 Jun 20; 99(4):319-326. PubMed ID: 30384382
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  • 18. Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson's disease in Serbia.
    Tomić A, Dobricić V, Novaković I, Svetel M, Pekmezović T, Kresojević N, Potrebić A, Kostić VS.
    Vojnosanit Pregl; 2013 May 20; 70(5):457-62. PubMed ID: 23789284
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  • 20. [Wilson disease: an update].
    Seo JK.
    Korean J Hepatol; 2006 Sep 20; 12(3):333-63. PubMed ID: 16998287
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