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323 related items for PubMed ID: 32791797

  • 1. [Phenotype and genotype analysis of 55 children patients with Wilson's disease].
    Zhou XY, Yin HX, Wang CL, Liu ZF, Zheng BX, Jin Y.
    Zhonghua Gan Zang Bing Za Zhi; 2020 Jul 20; 28(7):603-607. PubMed ID: 32791797
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  • 2. 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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  • 3. [Phenotypes and ATP7B gene variants in 316 children with Wilson disease].
    Lu ZK, Cheng J, Li SM, Lin YT, Zhang W, Li XZ, Sheng HY, Mao XJ, Mei HF, Zheng RD, Liang CL, Jiang MY, Huang YL, Liu L, Zeng CH.
    Zhonghua Er Ke Za Zhi; 2022 Apr 02; 60(4):317-322. PubMed ID: 35385937
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  • 5. [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 02; 41(1):35-8. PubMed ID: 14761325
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  • 10. Contribution of intragenic deletions to mutation spectrum in Chinese patients with Wilson's disease and possible mechanism underlying ATP7B gross deletions.
    Chen YC, Yu H, Wang RM, Xie JJ, Ni W, Zhang Y, Dong Y, Wu ZY.
    Parkinsonism Relat Disord; 2019 May 02; 62():128-133. PubMed ID: 30655162
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  • 11. ATP7B Mutation Detection and Pathogenicity Analysis: One Atypical Case of Wilson's Disease with Adrenocortical Insufficiency.
    Liu M, Jin M, Chen X, Wan B, Guo Y, Sheng M, Chen L, Zhao L, Huang D, Li Y.
    J Mol Neurosci; 2018 Jan 02; 64(1):20-28. PubMed ID: 29181760
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  • 14. 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 Jan 02; 11(12):e0168372. PubMed ID: 27992490
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  • 16. Presumed missense and synonymous mutations in ATP7B gene cause exon skipping in Wilson disease.
    Wang C, Zhou W, Huang Y, Yin H, Jin Y, Jia Z, Zhang A, Liu Z, Zheng B.
    Liver Int; 2018 Aug 02; 38(8):1504-1513. PubMed ID: 29637721
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  • 17. [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 02; 25(5):515-9. PubMed ID: 18841562
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  • 18. 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 02; 31(4):. PubMed ID: 27638368
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  • 20. [Mutational analysis of ATP7B gene of hepatolenticular degeneration in Xinjiang region].
    Aerziguli A, Li CZ, Hu LH, Lu XB, Sun XF.
    Zhonghua Gan Zang Bing Za Zhi; 2020 Aug 20; 28(8):699-702. PubMed ID: 32911910
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