載入...
Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature
Amyloid plaques formed by abnormal prion protein (PrP(Sc)) aggregates occur with low frequency in Creutzfeldt-Jakob disease, but represent a pathological hallmark of three relatively rare disease histotypes, namely variant CJD, sporadic CJDMV2K (methionine/valine at PRNP codon 129, PrP(Sc) type 2 an...
Na minha lista:
| 發表在: | Acta Neuropathol Commun |
|---|---|
| Main Authors: | , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BioMed Central
2017
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5701371/ https://ncbi.nlm.nih.gov/pubmed/29169405 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-017-0496-7 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|