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...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
Main Authors: Pastore, Manuela, Chin, Steven S., Bell, Karen L., Dong, Zhiqian, Yang, Qiwei, Yang, Lizhu, Yuan, Jue, Chen, Shu G., Gambetti, Pierluigi, Zou, Wen-Quan
Format: Artigo
Jezik:Inglês
Izdano: American Society for Investigative Pathology 2005
Teme:
Original Research Paper
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1613192/
https://ncbi.nlm.nih.gov/pubmed/16314483
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki