(Q47965426)

7 February 2018

title

Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease. (English)

1 reference

7 February 2018

author name string

Shibuya S

1

1 reference

7 February 2018

Higuchi J

2

1 reference

7 February 2018

Shin RW

3

1 reference

7 February 2018

Tateishi J

4

1 reference

7 February 2018

Kitamoto T

5

1 reference

7 February 2018

publication date

1 June 1998

1 reference

7 February 2018

published in

Annals of Neurology

1 reference

7 February 2018

volume

43

1 reference

7 February 2018

issue

6

1 reference

7 February 2018

page(s)

826-828

1 reference

7 February 2018

A protease-resistant protein is a structural component of the scrapie prion.

cites work

1 reference

https://api.crossref.org/works/10.1002%2FANA.410430618

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410430618

Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410430618

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410430618

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410430618

Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410430618

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410430618

21 January 2018

Identifiers

DOI

10.1002/ANA.410430618

1 reference

7 February 2018

PubMed ID

9629853

1 reference

7 February 2018