No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease

BACKGROUND: A polymorphism at codon 129 of the prion protein gene (PRNP) is the only well-known genetic risk factor for Creutzfeldt-Jakob disease (CJD). However, there is increasing evidence that other loci outside the PRNP open reading frame might play a role in CJD aetiology as well. METHODS: We s...

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Detalles Bibliográficos
Autores principales: Sánchez-Juan, Pascual, Bishop, Matthew T, Green, Alison, Giannattasio, Claudia, Arias-Vasquez, Alejandro, Poleggi, Anna, Knight, Richard SG, van Duijn, Cornelia M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2235832/
https://www.ncbi.nlm.nih.gov/pubmed/18072964
http://dx.doi.org/10.1186/1471-2350-8-77

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2235832/
https://www.ncbi.nlm.nih.gov/pubmed/18072964
http://dx.doi.org/10.1186/1471-2350-8-77

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