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Genetic PrP Prion Diseases
Genetic prion diseases (gPrDs) caused by mutations in the prion protein gene (PRNP) have been classified as genetic Creutzfeldt–Jakob disease, Gerstmann–Sträussler–Scheinker disease, or fatal familial insomnia. Mutations in PRNP can be missense, nonsense, and/or octapeptide repeat insertions or, pos...
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| Udgivet i: | Cold Spring Harb Perspect Biol |
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| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Cold Spring Harbor Laboratory Press
2018
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5932589/ https://ncbi.nlm.nih.gov/pubmed/28778873 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/cshperspect.a033134 |
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