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Journal Abstract Search

147 related items for PubMed ID: 20491539

  • 1. High prevalence of fulminant hepatic failure among patients with mutant alleles for truncation of ATP7B in Wilson's disease.
    Okada T, Shiono Y, Kaneko Y, Miwa K, Hasatani K, Hayashi Y, Mibayashi H, Aoyagi H, Tsuji S, Yoshimitsu M, Hayashi H, Yamagishi M.
    Scand J Gastroenterol; 2010 Oct; 45(10):1232-7. PubMed ID: 20491539
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  • 8. Intragenic Deletions in ATP7B as an Unusual Molecular Genetics Mechanism of Wilson's Disease Pathogenesis.
    Todorov T, Balakrishnan P, Savov A, Socha P, Schmidt HH.
    PLoS One; 2016 Oct; 11(12):e0168372. PubMed ID: 27992490
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  • 10. Genetic and Clinical Analysis in a Cohort of Patients with Wilson's Disease in Southwestern China.
    Liu Y, Zhou H, Guo H, Bai Y.
    Arch Med Res; 2015 Feb; 46(2):164-9. PubMed ID: 25704634
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  • 11. Molecular analysis and diagnosis in Japanese patients with Wilson's disease.
    Shimizu N, Nakazono H, Takeshita Y, Ikeda C, Fujii H, Watanabe A, Yamaguchi Y, Hemmi H, Shimatake H, Aoki T.
    Pediatr Int; 1999 Aug; 41(4):409-13. PubMed ID: 10453196
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  • 13. 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 Aug; 25(6):277-82. PubMed ID: 17264425
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  • 15. Mutational analysis of ATP7B and genotype-phenotype correlation in Japanese with Wilson's disease.
    Okada T, Shiono Y, Hayashi H, Satoh H, Sawada T, Suzuki A, Takeda Y, Yano M, Michitaka K, Onji M, Mabuchi H.
    Hum Mutat; 2000 Aug; 15(5):454-62. PubMed ID: 10790207
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  • 16. Wilson's disease in Southern Brazil: genotype-phenotype correlation and description of two novel mutations in ATP7B gene.
    Bem RS, Raskin S, Muzzillo DA, Deguti MM, Cançado EL, Araújo TF, Nakhle MC, Barbosa ER, Munhoz RP, Teive HA.
    Arq Neuropsiquiatr; 2013 Aug; 71(8):503-7. PubMed ID: 23982005
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  • 18. New mutations and polymorphisms of the ATP7B gene in sporadic Wilson disease.
    Lu CX, Qing Lin, Huang WQ, Tzeng CM.
    Eur J Med Genet; 2014 Sep; 57(9):498-502. PubMed ID: 24878384
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