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PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism

BACKGROUND: Genetic analysis of the human prion protein gene (PRNP) in suspect cases of Creutzfeldt-Jakob disease (CJD) is necessary for accurate diagnosis and case classification. Previous publications on the genetic variation at the PRNP locus have highlighted the presence of numerous polymorphism...

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Detalhes bibliográficos
Main Authors: Bishop, Matthew T, Pennington, Catherine, Heath, Craig A, Will, Robert G, Knight, Richard SG
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2806268/
https://ncbi.nlm.nih.gov/pubmed/20035629
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-10-146
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