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...

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Bibliografski detalji
Glavni autori: Bratosiewicz-Wąsik, Jolanta, Smoleń-Dzirba, Joanna, Rozemuller, Annemieke J., Jansen, Casper, Spliet, Wim, Jansen, Gerard H., Wąsik, Tomasz J., Liberski, Paweł P.
Format: Artigo
Jezik:Inglês
Izdano: Landes Bioscience 2012
Teme:
Research Paper
Online pristup: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
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