(Q37197688)

18 August 2017

0 references

Rare V203I mutation in the PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease (English)

1 reference

18 August 2017

1 reference

1

Qi Shi

1 reference

18 August 2017

10

Xiao-Ping Dong

1 reference

18 August 2017

Cao Chen

2

1 reference

18 August 2017

Xian-Jun Wang

3

1 reference

18 August 2017

Wei Zhou

4

1 reference

18 August 2017

Ji-Chun Wang

5

1 reference

18 August 2017

Bao-Yun Zhang

6

1 reference

18 August 2017

Chen Gao

7

1 reference

18 August 2017

Chen Gao

8

1 reference

18 August 2017

Jun Han

9

1 reference

18 August 2017

language of work or name

1 reference

1 May 2013

1 reference

18 August 2017

1 reference

18 August 2017

7

1 reference

18 August 2017

3

1 reference

18 August 2017

259-262

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3783113

18 August 2017

1 reference

Prion protein NMR structure and familial human spongiform encephalopathies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3783113

EEG abnormalities in poikilothermia suggesting Creutzfeldt-Jakob disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3783113

Clinical and familial characteristics of eight Chinese patients with T188K genetic Creutzfeldt-Jakob disease

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3783113

Clinical and familial characteristics of ten chinese patients with fatal family insomnia

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3783113

Sporadic Creutzfeldt-Jakob disease: a description of two cases.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3783113

Creutzfeldt-Jakob disease with the V203I mutation and M129V polymorphism of the prion protein gene (PRNP) and a 17 kDa prion protein fragment

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3783113

Age of onset and death in inherited prion disease are heritable

3 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.4161%2FPRI.24674

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

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23764840

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Creutzfeldt-Jakob Disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23764840

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.4161/PRI.24674

1 reference

18 August 2017

1 reference

18 August 2017

1 reference