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Pathological progression of genetic Creutzfeldt–Jakob disease with a PrP V180I mutation
In comparison to sporadic Creutzfeldt–Jakob disease (sCJD) with MM1-type and MM2- cortical (MM2C)-type, genetic CJD with a prion protein gene V180I mutation (V180I gCJD) is clinically characterized by onset at an older age, slower progress, and the absence of visual disturbances or cerebellar sympto...
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| Publicado no: | Prion |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5871029/ https://ncbi.nlm.nih.gov/pubmed/29264994 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336896.2017.1414130 |
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