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Journal Abstract Search

199 related items for PubMed ID: 18841562

  • 1. [Rapid detection of common ATP7B mutations in Wilson disease by high resolution melting analysis].
    Zhao X, Liu Y, Huang S, Meng Y, Sun M, Yang W, Zhang X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):515-9. PubMed ID: 18841562
    [Abstract] [Full Text] [Related]

  • 2. [Genotype and phenotype correlation in Chinese patients with Wilson's Disease].
    Liu XQ, Zhang YF, Liu TT, Gu XF, Hsiao KJ, Bao KR, Yu LH.
    Zhonghua Er Ke Za Zhi; 2003 Jan; 41(1):35-8. PubMed ID: 14761325
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  • 3. Development and evaluation of an unlabeled probe high-resolution melting assay for detection of ATP7B mutations in Wilson's disease.
    Xu A, Lv T, Zhang B, Zhang W, Ou X, Huang J.
    J Clin Lab Anal; 2017 Jul; 31(4):. PubMed ID: 27638368
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  • 4. Correlation of ATP7B genotype with phenotype in Chinese patients with Wilson disease.
    Liu XQ, Zhang YF, Liu TT, Hsiao KJ, Zhang JM, Gu XF, Bao KR, Yu LH, Wang MX.
    World J Gastroenterol; 2004 Feb 15; 10(4):590-3. PubMed ID: 14966923
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  • 5. Development of a high-resolution melting method for the screening of Wilson disease-related ATP7B gene mutations.
    Lin CW, Er TK, Tsai FJ, Liu TC, Shin PY, Chang JG.
    Clin Chim Acta; 2010 Sep 06; 411(17-18):1223-31. PubMed ID: 20465995
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  • 6. Detection of His1069Gln mutation in Wilson disease by bidirectional PCR amplification of specific alleles (BI-PASA) test.
    Poláková H, Katrincsáková B, Minárik G, Feráková E, Ficek A, Baldovic M, Kádasi L.
    Gen Physiol Biophys; 2007 Jun 06; 26(2):91-6. PubMed ID: 17660582
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  • 9. Identification of novel mutations and the three most common mutations in the human ATP7B gene of Korean patients with Wilson disease.
    Yoo HW.
    Genet Med; 2002 Jun 06; 4(6 Suppl):43S-48S. PubMed ID: 12544487
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  • 10. Genotyping microarray as a novel approach for the detection of ATP7B gene mutations in patients with Wilson disease.
    Gojová L, Jansová E, Külm M, Pouchlá S, Kozák L.
    Clin Genet; 2008 May 06; 73(5):441-52. PubMed ID: 18371106
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  • 11. Allele dropout in PCR-based diagnosis of Wilson disease: mechanisms and solutions.
    Lam CW, Mak CM.
    Clin Chem; 2006 Mar 06; 52(3):517-20. PubMed ID: 16510432
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  • 12. Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD).
    Seidel J, Caca K, Schwab SG, Berr F, Wildenauer DB, Mentzel HJ, Horn N, Kauf E.
    Cell Mol Biol (Noisy-le-grand); 2001 Mar 06; 47 Online Pub():OL149-57. PubMed ID: 11936861
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  • 16. Mutation analysis of the ATP7B gene and genotype-phenotype correlation in Chinese patients with Wilson disease.
    Li M, Ma J, Wang W, Yang X, Luo K.
    BMC Gastroenterol; 2021 Sep 01; 21(1):339. PubMed ID: 34470610
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  • 17. 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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  • 18. Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patients.
    Deguti MM, Genschel J, Cancado EL, Barbosa ER, Bochow B, Mucenic M, Porta G, Lochs H, Carrilho FJ, Schmidt HH.
    Hum Mutat; 2004 Apr 23; 23(4):398. PubMed ID: 15024742
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  • 20. ATP7B Gene Mutations in Croatian Patients with Wilson Disease.
    Ljubić H, Kalauz M, Telarović S, Ferenci P, Ostojić R, Noli MC, Lepori MB, Hrstić I, Vuković J, Premužić M, Radić D, Ravić KG, Sertić J, Merkler A, Barišić AA, Loudianos G, Vucelić B.
    Genet Test Mol Biomarkers; 2016 Mar 23; 20(3):112-7. PubMed ID: 26799313
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