Lataa...

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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Int J Mol Sci
Päätekijät: Wang, Pei-Wen, Lin, Tung-Yi, Hung, Yu-Chiang, Chang, Wen-Neng, Yang, Pei-Ming, Chen, Mu-Hong, Yeh, Chau-Ting, Pan, Tai-Long
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: MDPI 2019
Aiheet:
Linkit: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
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!