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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 Publishing Group
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3029211/ https://ncbi.nlm.nih.gov/pubmed/21686549 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr.09.2008.0945 |
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