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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Enregistré dans:
Détails bibliographiques
Publié dans:Brain Pathol
Auteurs principaux: Kobayashi, Atsushi, Matsuura, Yuichi, Iwaki, Toru, Iwasaki, Yasushi, Yoshida, Mari, Takahashi, Hitoshi, Murayama, Shigeo, Takao, Masaki, Kato, Shinsuke, Yamada, Masahito, Mohri, Shirou, Kitamoto, Tetsuyuki
Format: Artigo
Langue:Inglês
Publié: John Wiley and Sons Inc. 2015
Sujets:
Research Articles
Accès en ligne: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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