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Epidemiological characteristics of human prion diseases

Human prion diseases are a group of transmissible, progressive, and invariably fatal neurodegenerative disorders, which include Kuru, Creutzfeldt-Jakob disease (CJD), Gerstmann-Sträussler-Scheinker syndrome, and fatal familial insomnia. Human prion diseases affect approximately 1–2 persons per milli...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Infect Dis Poverty
Egile Nagusiak: Chen, Cao, Dong, Xiao-Ping
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2016
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4890484/
https://ncbi.nlm.nih.gov/pubmed/27251305
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40249-016-0143-8
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