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Sporadic Creutzfeldt-Jakob Disease and Other Proteinopathies in Comorbidity
Background: Sporadic Creutzfeldt–Jakob disease (sCJD) is the most common type of a group of transmissible spongiform encephalopathies (prion diseases). The etiology of the sporadic form of CJD is still unclear. sCJD can occur in combination with other neurodegenerative diseases, which further compli...
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| Vydáno v: | Front Neurol |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Frontiers Media S.A.
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7735378/ https://ncbi.nlm.nih.gov/pubmed/33329348 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2020.596108 |
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