Polymorphisms of the PRNP gene in Chinese populations and the identification of a novel insertion mutation (Q80363678)

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30 December 2019

title

Polymorphisms of the PRNP gene in Chinese populations and the identification of a novel insertion mutation (English)

1 reference

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30 December 2019

author name string

Shui-Liang Yu

1

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30 December 2019

Lei Jin

2

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30 December 2019

Man-Sun Sy

3

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30 December 2019

Fang-Hua Mei

4

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30 December 2019

Shu-Li Kang

5

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30 December 2019

Gui-Hong Sun

6

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30 December 2019

Po Tien

7

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30 December 2019

Fu-Sheng Wang

8

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30 December 2019

Geng-Fu Xiao

9

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publication date

1 October 2004

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European Journal of Human Genetics

30 December 2019

published in

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volume

12

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30 December 2019

issue

10

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page(s)

867-870

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201245

30 December 2019

exact match

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cites work

Molecular genetics of human prion diseases in Germany.

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7 January 2021

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

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Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

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

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7 January 2021

Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease

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7 January 2021

Bovine spongiform encephalopathy and variant Creutzfeldt-Jakob disease: background, evolution, and current concerns

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7 January 2021

Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics

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7 January 2021

Protective prion protein polymorphisms against sporadic Creutzfeldt-Jakob disease

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7 January 2021

Prion susceptibility and protective alleles exhibit marked geographic differences

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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7 January 2021

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

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7 January 2021

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

1 reference

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7 January 2021

Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1.

1 reference

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7 January 2021

Diversity at eight polymorphic Alu insertion loci in Chinese populations shows evidence for European admixture in an ethnic minority population from northwest China

1 reference

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7 January 2021

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

1 reference

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7 January 2021

The cellular prion protein binds copper in vivo

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7 January 2021

The prion protein and neuronal zinc homeostasis

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7 January 2021

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene

1 reference

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7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201245

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15266305%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

1 reference