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...

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Detalles Bibliográficos
Autores principales: Wang, Pei-Wen, Lin, Tung-Yi, Hung, Yu-Chiang, Chang, Wen-Neng, Yang, Pei-Ming, Chen, Mu-Hong, Yeh, Chau-Ting, Pan, Tai-Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770682/
https://www.ncbi.nlm.nih.gov/pubmed/31547461
http://dx.doi.org/10.3390/ijms20184528

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770682/
https://www.ncbi.nlm.nih.gov/pubmed/31547461
http://dx.doi.org/10.3390/ijms20184528

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