(Q42590888)

3 November 2017

Codon 219 polymorphism of PRNP in healthy Caucasians and Creutzfeldt-Jakob disease patients (English)

1 reference

Creutzfeldt-Jakob disease

3 November 2017

1 reference

Petraroli R

1

1 reference

3 November 2017

Pocchiari M

series ordinal

2

1 reference

3 November 2017

language of work or name

English

0 references

publication date

1 April 1996

1 reference

American Journal of Human Genetics

3 November 2017

1 reference

3 November 2017

58

1 reference

3 November 2017

4

1 reference

3 November 2017

888-889

1 reference

The original Gerstmann-Sträussler-Scheinker family of Austria: divergent clinicopathological phenotypes but constant PrP genotype

3 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914686

Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicine

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914686

Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD).

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914686

A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914686

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

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914686

Codon 129 changes in the prion protein gene in Caucasians

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914686

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914686

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914686

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914686

Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914686

Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914686

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914686

Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914686

New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome

16 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8644754

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/8644754

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The transmissible spongiform encephalopathies

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8644754

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

3 November 2017

PubMed publication ID

8644754

1 reference