Characterization of Fibrinogen as a Key Modulator in Patients with Wilson’s Diseases with Functional Proteomic Tools

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 basal ganglia. Although WD can be effectively treated with proper medicine...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Int J Mol Sci
Prif Awduron: Wang, Pei-Wen, Lin, Tung-Yi, Hung, Yu-Chiang, Chang, Wen-Neng, Yang, Pei-Ming, Chen, Mu-Hong, Yeh, Chau-Ting, Pan, Tai-Long
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: MDPI 2019
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6770682/
https://ncbi.nlm.nih.gov/pubmed/31547461
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms20184528
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