Characterization of mutations in PRNP (prion) gene and their possible roles in neurodegenerative diseases

Abnormal prion proteins are responsible for several fatal neurodegenerative diseases in humans and in animals, including Creutzfeldt–Jakob disease (CJD), Gerstmann–Sträussler–Scheinker disease, and fatal familial insomnia. Genetics is important in prion diseases, but in the most cases, cause of dise...

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Detalles Bibliográficos
Autores principales: Bagyinszky, Eva, Giau, Vo Van, Youn, Young Chul, An, Seong Soo A, Kim, SangYun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097508/
https://www.ncbi.nlm.nih.gov/pubmed/30147320
http://dx.doi.org/10.2147/NDT.S165445

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097508/
https://www.ncbi.nlm.nih.gov/pubmed/30147320
http://dx.doi.org/10.2147/NDT.S165445

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