The genetic Creutzfeldt-Jakob disease with E200K mutation: analysis of clinical, genetic and laboratory features of 30 Chinese patients

Genetic Creutzfeldt-Jakob disease (gCJD) with E200K mutation is one of the common subtypes of human genetic prion diseases worldwide. In this study, we systematically analyzed 30 Chinese E200K gCJD cases for their epidemiological, clinical, laboratory and genetic features. The patients came from 12...

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Detalles Bibliográficos
Autores principales: Gao, Li-Ping, Shi, Qi, Xiao, Kang, Wang, Jing, Zhou, Wei, Chen, Cao, Dong, Xiao-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372685/
https://www.ncbi.nlm.nih.gov/pubmed/30755683
http://dx.doi.org/10.1038/s41598-019-38520-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372685/
https://www.ncbi.nlm.nih.gov/pubmed/30755683
http://dx.doi.org/10.1038/s41598-019-38520-y

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