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Autor:
Kang Xiao, Ming-Fan Pang, Yue-Qiao Zhao, Li-Ping Gao, Yue-Zhang Wu, Yuan Wang, Qi Shi, Xiao-Ping Dong
Publikováno v:
Prion, Vol 16, Iss 1, Pp 58-65 (2022)
Human prion diseases (PrDs) are a group of transmissible neurodegenerative diseases that can be clarified as sporadic, genetic and iatrogenic forms. In this study, we have analysed the time and geographic distributions of 2011 PrD cases diagnosed by
Externí odkaz:
https://doaj.org/article/3ee9f106dfd24b8295dd46dea21f175f