Rare genetic Creutzfeldt-Jakob disease with E196A mutation: a case report
Author:
Affiliation:
1. Department of Neurology, Neuroscience Center, The First Hospital of Jilin University, Jilin University, Changchun, China
Funder
the Chinese National Natural Science Foundation
Publisher
Informa UK Limited
Subject
Infectious Diseases,Cell Biology,Cellular and Molecular Neuroscience,Biochemistry
Link
https://tandfonline.com/doi/pdf/10.1080/19336896.2019.1631679
Reference16 articles.
1. Hereditary Human Prion Diseases: an Update
2. Genetic Studies in Human Prion Diseases
3. A Unifying Role for Prions in Neurodegenerative Diseases
4. Genetic PrP Prion Diseases
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