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Aggregation of prion protein with insertion mutations is proportional to the number of inserts
Mutation in the prion gene, PRNP, accounts for approx. 10–15% of human prion diseases. However, little is known about the mechanisms by which a mutant prion protein (PrP) causes disease. We compared the biochemical properties of a wild-type human prion protein, rPrP(C) (recombinant wild-type PrP), w...
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| Main Authors: | , , , , , , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Portland Press Ltd.
2007
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1874237/ https://ncbi.nlm.nih.gov/pubmed/17187581 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BJ20061592 |
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