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Editorial
. 2021 Dec;17(6):561-565.
doi: 10.1007/s12519-021-00475-4. Epub 2021 Oct 29.

Challenges and suggestions for precise diagnosis and treatment of Wilson's disease

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Editorial

Challenges and suggestions for precise diagnosis and treatment of Wilson's disease

Yi Dong et al. World J Pediatr. 2021 Dec.
No abstract available

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References

    1. Bull PC, Thomas GR, Rommens JM, Forbes JR, Cox DW. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nat Genet. 1993;5:327–37. - DOI
    1. Petrukhin K, Fischer SG, Pirastu M, Tanzi RE, Chernov I, Devoto M, et al. Mapping, cloning and genetic characterization of the region containing the Wilson disease gene. Nat Genet. 1993;5:338–43. - DOI
    1. Tanzi RE, Petrukhin K, Chernov I, Pellequer JL, Wasco W, Ross B, et al. The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene. Nat Genet. 1993;5:344–50. - DOI
    1. Roberts EA, Schilsky ML, American Association for Study of Liver D. Diagnosis and treatment of Wilson disease: an update. Hepatology. 2008;47:2089. - DOI
    1. European Association for Study of L. EASL clinical practice guidelines: Wilson's disease. J Hepatol 2012;56:671–685. - DOI

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