Sporadic Creutzfeldt–Jakob Disease MM1+2C and MM1 are Identical in Transmission Properties

The genotype (methionine, M or valine, V) at polymorphic codon 129 of the PRNP gene and the type (1 or 2) of abnormal prion protein in the brain are the major determinants of the clinicopathological features of sporadic Creutzfeldt–Jakob disease (CJD), thus providing molecular basis for classificati...

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Uloženo v:
Podrobná bibliografie
Vydáno v:Brain Pathol
Hlavní autoři: Kobayashi, Atsushi, Matsuura, Yuichi, Iwaki, Toru, Iwasaki, Yasushi, Yoshida, Mari, Takahashi, Hitoshi, Murayama, Shigeo, Takao, Masaki, Kato, Shinsuke, Yamada, Masahito, Mohri, Shirou, Kitamoto, Tetsuyuki
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2015
Témata:
Research Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8028929/
https://ncbi.nlm.nih.gov/pubmed/25851836
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bpa.12264
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