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Creutzfeldt-Jakob disease associated with a missense mutation at codon 200 of the prion protein gene in Brazil
Genetic Creutzfeldt-Jakob disease (gCJD) represents less than 15% of CJD cases, and its clinical picture may be either indistinguishable from that of sporadic CJD (sCJD) or be atypical, usually with younger onset and longer duration. We report a case of 59-year old Brazilian man who presented rapidl...
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| Publicado no: | Dement Neuropsychol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Associação de Neurologia Cognitiva e do
Comportamento
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5619573/ https://ncbi.nlm.nih.gov/pubmed/29213392 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/s1980-57642008dn10200017 |
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