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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Bibliografski detalji
Glavni autori: Sanchez-Juan, Pascual, Bishop , Matthew T, Croes , Esther A, Knight , Richard SG, Will , Robert G, van Duijn , Cornelia M, Manson , Jean C
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2011
Teme:
Research Article
Online pristup: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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