Clinical and Laboratory Features of Three Rare Chinese V210I gCJD Patients

Genetic human prion diseases are a group of inherited encephalopathies directly associated with different mutations in PrP-encoding gene PRNP, including more than 50 different mutations worldwide. Some genotypes of mutations show ethno-correlation, and among them, genetic Creutzfeldt–Jacob disease (...

Descripción completa

Detalles Bibliográficos
Autores principales: Xiao, Kang, Zhou, Wei, Gao, Li-Ping, Wu, Yue-Zhang, Wang, Yuan, Chen, Cao, Gao, Chen, Shi, Qi, Dong, Xiao-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601525/
https://www.ncbi.nlm.nih.gov/pubmed/32998248
http://dx.doi.org/10.3390/pathogens9100800

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601525/
https://www.ncbi.nlm.nih.gov/pubmed/32998248
http://dx.doi.org/10.3390/pathogens9100800

Ejemplares similares