A Chinese Creutzfeldt-Jakob disease patient with E196K mutation inPRNP-Reference-Cited by-同舟云学术

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A Chinese Creutzfeldt-Jakob disease patient with E196K mutation inPRNP

Published:2011-04 Issue:2 Volume:5 Page:117-120
ISSN:1933-6896
Container-title:Prion
language:en
Short-container-title:Prion

Author:

Shi Qi,Chen Cao,Song Xiao-Nan,Gao Chen,Tian Chan,Zhou Wei,Song Xu-Hua,Yao Lai-Shun,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.5.2.15846

Reference17 articles.

1. Nobel Lecture: Prions

2. Clinical aspects of human spongiform encephalopathies, with the exception of iatrogenic forms

3. Genetic Creutzfeldt–Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis

4. Pathogenesis and prevalence of variant Creutzfeldt-Jakob disease

5. Human Prion disease with a T188K mutation in Chinese: a case report

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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. Characteristics of Chinese patients with genetic CJD who have E196A or E196K mutation in PRNP: comparative analysis of patients identified in the Chinese National CJD Surveillance System;BMJ Open;2021-11

5. Probable genetic Creutzfeldt-Jakob Disease with rare E196K mutation;Neurologia i Neurochirurgia Polska;2021-02-28

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