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A novel phenotype of sporadic Creutzfeldt–Jakob disease
An atypical case of sporadic Creutzfeldt–Jakob disease (CJD) is described in a 78‐year‐old woman homozygous for methionine at codon 129 of the prion protein (PrP) gene. The neuropathological signature was the presence of PrP immunoreactive plaque‐like deposits in the cerebral cortex, striatum and th...
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| Main Authors: | , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Group
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2095610/ https://ncbi.nlm.nih.gov/pubmed/18024694 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.2007.115444 |
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