(Q43882689)

27 November 2017

title

Distribution of the M129V polymorphism of the prion protein gene in a Turkish population suggests a high risk for Creutzfeldt-Jakob disease (English)

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27 November 2017

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Nihan Erginel-Unaltuna

1

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27 November 2017

Peoc'h K

2

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27 November 2017

Komurcu E

3

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27 November 2017

Acuner TT

4

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27 November 2017

Issever H

5

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27 November 2017

Laplanche JL

6

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27 November 2017

publication date

1 December 2001

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European Journal of Human Genetics

27 November 2017

published in

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27 November 2017

volume

9

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27 November 2017

issue

12

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27 November 2017

page(s)

965-968

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Shattuck lecture--neurodegenerative diseases and prions

27 November 2017

cites work

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

The new variant of Creutzfeldt-Jakob disease.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

1 reference

7 January 2021

Lack of evidence to support the association of the human prion gene with schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

Sequence variation in intron of prion protein gene, crucial for complete diagnostic strategies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

Deletion in prion protein gene in a Moroccan family

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

Deletions in the prion protein gene are not associated with CJD.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

Polymorphism at codon 129 of the prion protein gene is not associated with sporadic AD

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

Genotyping of the prion protein gene at codon 129

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

Genotype at codon 129 and susceptibility to Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200754

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5200754

1 reference

Dimensions Publication ID

27 November 2017

1038098588

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1 reference