Association between the PRNP 1368 polymorphism and the occurrence of sporadic Creutzfeldt-Jakob disease

Creutzfeldt-Jakob disease (CJD) is a rare transmissible neurodegenerative disorder. The etiology of sporadic form of CJD remains unsolved. In addition to the codon 129 polymorphism, polymorphisms in the non-coding region of PRNP are considered as important factors in sCJD development. To assess a po...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Bratosiewicz-Wąsik, Jolanta, Smoleń-Dzirba, Joanna, Rozemuller, Annemieke J., Jansen, Casper, Spliet, Wim, Jansen, Gerard H., Wąsik, Tomasz J., Liberski, Paweł P.
Formato: Artigo
Lenguaje:Inglês
Publicado: Landes Bioscience 2012
Materias:
Research Paper
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3609072/
https://ncbi.nlm.nih.gov/pubmed/22895088
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/pri.21773
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares