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Clinical and Laboratory Features of Three Rare Chinese V210I gCJD Patients

Genetic human prion diseases are a group of inherited encephalopathies directly associated with different mutations in PrP-encoding gene PRNP, including more than 50 different mutations worldwide. Some genotypes of mutations show ethno-correlation, and among them, genetic Creutzfeldt–Jacob disease (...

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Detalles Bibliográficos
Autores principales:	Xiao, Kang, Zhou, Wei, Gao, Li-Ping, Wu, Yue-Zhang, Wang, Yuan, Chen, Cao, Gao, Chen, Shi, Qi, Dong, Xiao-Ping
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2020
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601525/ https://www.ncbi.nlm.nih.gov/pubmed/32998248 http://dx.doi.org/10.3390/pathogens9100800

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