Strain specific resistance to murine scrapie associated with a naturally occurring human prion protein polymorphism at residue 171.
Transmissible spongiform encephalopathies (TSE) or prion diseases are neurodegenerative disorders associated with conversion of normal host prion protein (PrP) to a misfolded, protease-resistant form (PrPres). Genetic variations of prion protein in humans and animals can alter susceptibility to both...
Main Authors: | James F Striebel, Brent Race, Kimberly D Meade-White, Rachel LaCasse, Bruce Chesebro |
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Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2011-09-01
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Series: | PLoS Pathogens |
Online Access: | http://europepmc.org/articles/PMC3182929?pdf=render |
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