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Transmission characteristics of heterozygous cases of Creutzfeldt-Jakob disease with variable abnormal prion protein allotypes

In the human prion disease Creutzfeldt-Jakob disease (CJD), different CJD neuropathological subtypes are defined by the presence in normal prion protein (PrP(C)) of a methionine or valine at residue 129, by the molecular mass of the infectious prion protein PrP(Sc), by the pattern of PrP(Sc) deposit...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Acta Neuropathol Commun
Egile Nagusiak: Ward, Anne, Hollister, Jason R., McNally, Kristin, Ritchie, Diane L., Zanusso, Gianluigi, Priola, Suzette A.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2020
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC7285538/
https://ncbi.nlm.nih.gov/pubmed/32517816
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-020-00958-x
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