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Unusual presentations in patients with E200K familial Creutzfeldt-Jakob Disease
BACKGROUND AND PROPOSE: Familial Creutzfeldt-Jakob disease (fCJD) in Jews of Libyan ancestry is caused by an E200K mutation in the PRNP gene. The typical presenting symptoms include cognitive decline, behavioral changes and gait disturbances, however some patients may have an unusual presentation su...
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| Yayımlandı: | Eur J Neurol |
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| Asıl Yazarlar: | , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4833540/ https://ncbi.nlm.nih.gov/pubmed/26806765 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ene.12955 |
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