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...

Descripción completa

Detalles Bibliográficos
Autores principales: Sanchez-Juan, Pascual, Bishop , Matthew T, Croes , Esther A, Knight , Richard SG, Will , Robert G, van Duijn , Cornelia M, Manson , Jean C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114709/
https://www.ncbi.nlm.nih.gov/pubmed/21600043
http://dx.doi.org/10.1186/1471-2350-12-73

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114709/
https://www.ncbi.nlm.nih.gov/pubmed/21600043
http://dx.doi.org/10.1186/1471-2350-12-73

Ejemplares similares