Prion protein codon 129 polymorphism in mild cognitive impairment and dementia: the Rotterdam Study

Creutzfeldt–Jakob disease is a rare, fatal, neurodegenerative disease caused by the accumulation of abnormally folded prion proteins. The common polymorphism at codon 129 (methionine/valine) in the prion protein (PRNP) gene is the most important determinant of genetic susceptibility. Homozygotes of...

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Detalles Bibliográficos
Autores principales: Karamujić-Čomić, Hata, Ahmad, Shahzad, Lysen, Thom S, Heshmatollah, Alis, Roshchupkin, Gennady V, Vernooij, Meike W, Rozemuller, Annemieke J M, Ikram, Mohammad Arfan, Amin, Najaf, van Duijn, Cornelia M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425338/
https://www.ncbi.nlm.nih.gov/pubmed/32954288
http://dx.doi.org/10.1093/braincomms/fcaa030

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425338/
https://www.ncbi.nlm.nih.gov/pubmed/32954288
http://dx.doi.org/10.1093/braincomms/fcaa030

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