Familial Creutzfeldt–Jakob Disease: The First Reported Kindred from South-East Asia

Creutzfeldt–Jakob disease (CJD) belongs to a group of prion disease that is caused by abnormally folded proteins and is clinically characterized by rapidly progressive cognitive decline, gait abnormalities, and myoclonus. Familial CJD is very rare and is described only in few families around the wor...

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Detalles Bibliográficos
Autores principales: Sawal, Nishit, Chakravarty, Kamalesh, Puri, Inder, Goyal, Vinay, Garg, Ajay, Shi, Qi, Zhou, Wei, Xiaoping, Dong, Shukla, Garima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6472217/
https://www.ncbi.nlm.nih.gov/pubmed/31007442
http://dx.doi.org/10.4103/aian.AIAN_441_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6472217/
https://www.ncbi.nlm.nih.gov/pubmed/31007442
http://dx.doi.org/10.4103/aian.AIAN_441_18

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