Prion Mutations in Republic of Republic of Korea, China, and Japan

Prion gene (PRNP) mutations are associated with diverse disease phenotypes, including familiar Creutzfeldt–Jakob Disease (CJD), Gerstmann–Sträussler–Scheinker disease (GSS), and fatal familial insomnia (FFI). Interestingly, PRNP mutations have been reported in patients diagnosed with Alzheimer’s dis...

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Detalles Bibliográficos
Autores principales: Kim, Dan Yeong, Shim, Kyu Hwan, Bagyinszky, Eva, An, Seong Soo A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9820783/
https://www.ncbi.nlm.nih.gov/pubmed/36614069
http://dx.doi.org/10.3390/ijms24010625

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9820783/
https://www.ncbi.nlm.nih.gov/pubmed/36614069
http://dx.doi.org/10.3390/ijms24010625

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