A polymorphism in the regulatory region of PRNP is associated with increased risk of sporadic Creutzfeldt-Jakob disease
about
Genetic studies in human prion diseases.Age at Death of Creutzfeldt-Jakob disease in subsequent family generation carrying the E200K mutation of the prion protein gene.Lack of association of the M129V polymorphism of the PRNP gene with pseudoexfoliation syndrome.Identification of a novel endoplasmic reticulum stress response element regulated by XBP1.Scientific Opinion on a request for a review of a scientific publication concerning the zoonotic potential of ovine scrapie prions
P2860
A polymorphism in the regulatory region of PRNP is associated with increased risk of sporadic Creutzfeldt-Jakob disease
description
2011 nî lūn-bûn
@nan
2011 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
A polymorphism in the regulato ...... adic Creutzfeldt-Jakob disease
@ast
A polymorphism in the regulato ...... adic Creutzfeldt-Jakob disease
@en
type
label
A polymorphism in the regulato ...... adic Creutzfeldt-Jakob disease
@ast
A polymorphism in the regulato ...... adic Creutzfeldt-Jakob disease
@en
prefLabel
A polymorphism in the regulato ...... adic Creutzfeldt-Jakob disease
@ast
A polymorphism in the regulato ...... adic Creutzfeldt-Jakob disease
@en
P2093
P2860
P356
P1433
P1476
A polymorphism in the regulato ...... adic Creutzfeldt-Jakob disease
@en
P2093
Esther A Croes
Jean C Manson
Matthew T Bishop
Pascual Sanchez-Juan
Richard Sg Knight
Robert G Will
P2860
P2888
P356
10.1186/1471-2350-12-73
P577
2011-05-22T00:00:00Z
P5875
P6179
1032537666