Rare V203I mutation in thePRNPgene of a Chinese patient with Creutzfeldt–Jakob disease-Reference-Cited by-同舟云学术

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Rare V203I mutation in thePRNPgene of a Chinese patient with Creutzfeldt–Jakob disease

Published:2013-05 Issue:3 Volume:7 Page:259-262
ISSN:1933-6896
Container-title:Prion
language:en
Short-container-title:Prion

Author:

Shi Qi,Chen Cao,Wang Xian-Jun,Zhou Wei,Wang Ji-Chun,Zhang Bao-Yun,Tian Chan,Gao Chen,Han Jun,Dong Xiao-Ping

Publisher

Informa UK Limited

Subject

Infectious Diseases,Cell Biology,Cellular and Molecular Neuroscience,Biochemistry

Link

http://www.tandfonline.com/doi/pdf/10.4161/pri.24674

Reference10 articles.

1. Nobel Lecture: Prions

2. Creutzfeldt-Jakob Disease

3. Clinical and familial characteristics of eight Chinese patients with T188K genetic Creutzfeldt–Jakob disease

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

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1. A systemic analysis of Creutzfeldt Jakob disease cases in Asia;Prion;2024-02-07

2. Prion Mutations in Republic of Republic of Korea, China, and Japan;International Journal of Molecular Sciences;2022-12-30

3. Characteristics of Different Types of Prion Diseases - China's Surveillance;CHINA CDC WEEKLY;2022

4. Penetrance of the V203I variant of the PRNP gene: report of a patient with stroke-like onset of Creutzfeld-Jacob Disease and review of published cases;Prion;2022-02-15

5. Myoclonus‐Ataxia Syndromes: A Diagnostic Approach;Movement Disorders Clinical Practice;2020-11-03

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