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

OBJECTIVE: Two different mutations at codon 196, namely E196A and E196K, have been reported to be related to genetic Creutzfeldt-Jakob disease (CJD). We aimed to comparatively analyse the features of Chinese patients with these two mutations from the CJD surveillance system in China. DESIGN AND SETT...

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Detalles Bibliográficos
Autores principales: Shi, Qi, Xiao, Kang, Chen, Cao, Zhou, Wei, Gao, Li-Ping, Wu, Yue-Zhang, Wang, Yuan, Hu, Chao, Gao, Chen, Dong, Xiao-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593757/
https://www.ncbi.nlm.nih.gov/pubmed/34782343
http://dx.doi.org/10.1136/bmjopen-2021-054551

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