Rare genetic Creutzfeldt-Jakob disease with T188K mutation: analysis of clinical, genetic and laboratory features of30 Chinese patients-Reference-Cited by-同舟云学术

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Rare genetic Creutzfeldt-Jakob disease with T188K mutation: analysis of clinical, genetic and laboratory features of30 Chinese patients

Published:2017-03-17 Issue:10 Volume:88 Page:889-890
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:J Neurol Neurosurg Psychiatry

Author:

Shi Qi,Zhou Wei,Chen Cao,Xiao Kang,Wang Yuan,Gao Chen,Dong Xiao-Ping

Funder

National Key Research and Development Plan

SKLID Development Grant

Chinese National Natural Science Foundation Grants

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference5 articles.

1. High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes;Finckh;Am J Hum Genet,2000

2. Human prion disease with a T188K mutation in Chinese: a case report;Shi;Cases J,2009

3. The features of genetic prion diseases based on Chinese surveillance program;Shi;PLoS One,2015

4. Clinical and familial characteristics of eight Chinese patients with T188K genetic Creutzfeldt-Jakob disease;Chen;Infect Genet Evol,2013

5. Prospective 10-year surveillance of human prion diseases in Japan;Nozaki;Brain,2010

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

2. Spontaneous prion disease in homozygous and heterozygous transgenic mouse models of T188K genetic Creutzfeldt-Jakob disease;Neurobiology of Aging;2023-11

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

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

5. Clinical and prognostic features of Heidenhain variant of Creutzfeldt−Jakob disease: A retrospective case series study;European Journal of Neurology;2022-05-17

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