Evidence for a Pathogenic Role of Different Mutations at Codon 188 of PRNP

Clinical and pathological changes in familial Creutzfeldt-Jakob disease (CJD) cases may be similar or indistinguishable from sporadic CJD. Therefore determination of novel mutations in PRNP remains of major importance. We identified two different rare mutations in codon 188 of the prion protein gene...

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Detalhes bibliográficos
Main Authors: Roeber, Sigrun, Grasbon-Frodl, Eva-Maria, Windl, Otto, Krebs, Bjarne, Xiang, Wei, Vollmert, Caren, Illig, Thomas, Schröter, Andreas, Arzberger, Thomas, Weber, Petra, Zerr, Inga, Kretzschmar, Hans A.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2008
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2366066/
https://ncbi.nlm.nih.gov/pubmed/18478114
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0002147
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