A polymorphism in the regulatory region of PRNP is associated with increased risk of sporadic Creutzfeldt-Jakob disease

BACKGROUND: Creutzfeldt-Jakob disease (CJD) is a rare transmissible neurodegenerative disorder. An important determinant for CJD risk and phenotype is the M129V polymorphism of the human prion protein gene (PRNP), but there are also other coding and non-coding polymorphisms inside this gene. METHODS...

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Bibliografiset tiedot
Päätekijät: Sanchez-Juan, Pascual, Bishop , Matthew T, Croes , Esther A, Knight , Richard SG, Will , Robert G, van Duijn , Cornelia M, Manson , Jean C
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2011
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3114709/
https://ncbi.nlm.nih.gov/pubmed/21600043
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-12-73
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