Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases
In man, mutations in different regions of the prion protein (PrP) are associated with infectious neurodegenerative diseases that have remarkably different clinical signs and neuropathological lesions. To explore the roots of this phenomenon, we created a knock-in mouse model carrying the mutation as...
| Main Authors: | , , , , , , |
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| Other Authors: | |
| Format: | Article |
| Language: | en_US |
| Published: |
National Academy of Sciences (U.S.)
2014
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| Online Access: | http://hdl.handle.net/1721.1/89098 https://orcid.org/0000-0002-2834-6359 https://orcid.org/0000-0003-1307-882X |