Characterization of Fibrinogen as a Key Modulator in Patients with Wilson’s Diseases with Functional Proteomic Tools
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DOI: 10.3390/ijms20184528
Abstract: Wilson’s disease (WD) is an autosomal recessive disorder of copper metabolism caused by defects in the ATPase gene (ATP7B). The various clinical features result from the massive accumulation of copper in the liver, cornea and… read more here.
Keywords: patients wilson; characterization fibrinogen; fibrinogen; key modulator ... See more keywords