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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Detalhes bibliográficos
Publicado no:Brain Pathol
Main Authors: Kobayashi, Atsushi, Matsuura, Yuichi, Iwaki, Toru, Iwasaki, Yasushi, Yoshida, Mari, Takahashi, Hitoshi, Murayama, Shigeo, Takao, Masaki, Kato, Shinsuke, Yamada, Masahito, Mohri, Shirou, Kitamoto, Tetsuyuki
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2015
Assuntos:
Research Articles
Acesso em linha: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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