Rare genetic Creutzfeldt-Jakob disease with E196A mutation: a case report

Genetic Creutzfeldt-Jakob disease (gCJD) accounts for approximately 10–15% of human prion diseases. It is an autosomal dominant disease caused by missense or insertion mutations of the gene that encodes prion protein (PRNP). In general, the manifestations and neuropathological changes of gCJD are si...

Descripción completa

Detalles Bibliográficos
Autores principales: Dai, Yanyuan, Lang, Yue, Ding, Mingxuan, Zhang, Baizhuo, Han, Xiaoou, Duan, Guangyu, Cui, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629187/
https://www.ncbi.nlm.nih.gov/pubmed/31238786
http://dx.doi.org/10.1080/19336896.2019.1631679

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629187/
https://www.ncbi.nlm.nih.gov/pubmed/31238786
http://dx.doi.org/10.1080/19336896.2019.1631679

Ejemplares similares