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117 related items for PubMed ID: 25365615

  • 1. The same haplotype for two unrelated Wilson disease patients with new ATP7B mutation.
    Dastsooz H, Dehghani SM, Fardaei M.
    Arch Iran Med; 2014 Nov; 17(11):755-8. PubMed ID: 25365615
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  • 5. Mutation analysis and characterization of alternative splice variants of the Wilson disease gene ATP7B.
    Wan L, Tsai CH, Hsu CM, Huang CC, Yang CC, Liao CC, Wu CC, Hsu YA, Lee CC, Liu SC, Lin WD, Tsai FJ.
    Hepatology; 2010 Nov; 52(5):1662-70. PubMed ID: 20931554
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  • 14. Identification of one novel and nine recurrent mutations of the ATP7B gene in 11 children with Wilson disease.
    Geng J, Wang J, Yao RE, Liu XQ, Fu QH.
    World J Pediatr; 2013 May; 9(2):158-62. PubMed ID: 23275100
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  • 15. Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association.
    Lee CC, Wu JY, Tsai FJ, Kodama H, Abe T, Yang CF, Tsai CH.
    J Hum Genet; 2000 May; 45(5):275-9. PubMed ID: 11043508
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  • 16. Identification of a high frequency of mutation at exon 8 of the ATP7B gene in a Chinese population with Wilson disease by fluorescent PCR.
    Xu P, Liang X, Jankovic J, Le W.
    Arch Neurol; 2001 Nov; 58(11):1879-82. PubMed ID: 11708998
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