Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease

A man was studied with sporadic Creutzfeldt-Jakob disease (sCJD) who had serial cortical syndromes evolving over 15 months without significant ataxia, prominent myoclonus, or periodic complexes on EEG examinations. This clinical phenotype correlated with a predominantly cortical and striatal distrib...

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Hlavní autoři: Worrall, B., Herman, S., Capellari, S., Lynch, T., Chin, S., Gambetti, P., Parchi, P.
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Group 1999
Témata:
Short Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1736644/
https://ncbi.nlm.nih.gov/pubmed/10519879
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