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Creutzfeldt-Jakob disease associated with a V203I homozygous mutation in the prion protein gene
We report a Japanese patient with Creutzfeldt-Jakob disease (CJD) with a V203I homozygous mutation of the prion protein gene (PRNP). A 73-year-old woman developed rapidly progressive gait disturbance and cognitive dysfunction. Four months after the onset, she entered a state of an akinetic mutism. G...
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| Publicado no: | Prion |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4601383/ https://ncbi.nlm.nih.gov/pubmed/25495585 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/19336896.2014.971569 |
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