טוען...
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 clinicalpicture 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 rapidly...
שמור ב:
| הוצא לאור ב: | Dementia & Neuropsychologia |
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| Main Authors: | , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Associação Neurologia Cognitiva e do Comportamento
2007
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| נושאים: | |
| גישה מקוונת: | https://www.redalyc.org/articulo.oa?id=339528998016 |
| תגים: |
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