Creutzfeldt-Jakob Disease (CJD) with a Mutation at Codon 148 of Prion Protein Gene : Relationship with Sporadic CJD

Creutzfeldt-Jakob disease (CJD), the most common human prion disease, includes sporadic (s) and familial (f) forms. Regardless of etiology, both forms are thought to share the pathogenic mechanism whereby the cellular prion protein (PrP(C)) converts into its pathogenic isoform (PrP(Sc)). While PrP(C...

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Detaylı Bibliyografya
Asıl Yazarlar: Pastore, Manuela, Chin, Steven S., Bell, Karen L., Dong, Zhiqian, Yang, Qiwei, Yang, Lizhu, Yuan, Jue, Chen, Shu G., Gambetti, Pierluigi, Zou, Wen-Quan
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Investigative Pathology 2005
Konular:
Original Research Paper
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1613192/
https://ncbi.nlm.nih.gov/pubmed/16314483
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