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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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| Publicado no: | Brain Pathol |
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| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2015
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| Assuntos: | |
| 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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