Creutzfeldt-Jakob disease: current issues (review)
Creutzfeldt-Jakob disease and others human prion diseases arefatal neurodegenerative conditions. Etiologic classificationincludes sporadic, hereditary and acquired forms.Conformational change of the normal (cellular) form of prionprotein (PrPc) to a pathological form (PrPSс) is considered centralto...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Research Center of Neurology
2017-02-01
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| Edice: | Анналы клинической и экспериментальной неврологии |
| Témata: | |
| On-line přístup: | https://annaly-nevrologii.com/journal/pathID/article/viewFile/278/344 |
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