Familial Creutzfeldt-Jakob Disease with V180I Mutation

Creutzfeldt-Jakob disease (CJD) is an uncommon neurodegenerative disorder with an incidence of 1 per 1000,000 per year typically characterized by rapidly progressive dementia, ataxia, myoclonus and behavioral changes. Genetic prion diseases, which develop due to a mutations in the prion protein gene...

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Detalles Bibliográficos
Autores principales: Yang, Tae-Il, Jung, Dae-Soo, Ahn, Bo-Young, Jeong, Byung-Hoon, Cho, Han-Jeong, Kim, Yong-Sun, Na, Duk L., Geschwind, Michael D., Kim, Eun-Joo
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890893/
https://www.ncbi.nlm.nih.gov/pubmed/20592908
http://dx.doi.org/10.3346/jkms.2010.25.7.1097

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890893/
https://www.ncbi.nlm.nih.gov/pubmed/20592908
http://dx.doi.org/10.3346/jkms.2010.25.7.1097

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