The first Chinese case of Creutzfeldt-Jakob disease patient with R208H mutation inPRNP
Author:
Publisher
Informa UK Limited
Subject
Infectious Diseases,Cell Biology,Cellular and Molecular Neuroscience,Biochemistry
Link
http://www.tandfonline.com/doi/pdf/10.4161/pri.5.3.16796
Reference4 articles.
1. Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease
2. Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene
3. Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment
4. Familial Creutzfeldt-Jakob Disease With an R208H-129V Haplotype and Kuru Plaques
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1. A systemic analysis of Creutzfeldt Jakob disease cases in Asia;Prion;2024-02-07
2. Characteristics of Different Types of Prion Diseases - China's Surveillance;CHINA CDC WEEKLY;2022
3. Genetic Creutzfeldt-Jakob disease in Sardinia: a case series linked to the PRNP R208H mutation due to a single founder effect;neurogenetics;2020-05-26
4. Characterization of mutations in PRNP (prion) gene and their possible roles in neurodegenerative diseases;Neuropsychiatric Disease and Treatment;2018-08
5. Genetic Creutzfeldt–Jakob disease;Human Prion Diseases;2018
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