Clinical and Laboratory Features of Three Rare Chinese V210I gCJD Patients

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 <i>PRNP</i>, including more than 50 different mutations worldwide. Some genotypes of mutations show ethno-correlation, and among them, genetic Creutzfe...

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Bibliographic Details
Main Authors:	Kang Xiao, Wei Zhou, Li-Ping Gao, Yue-Zhang Wu, Yuan Wang, Cao Chen, Chen Gao, Qi Shi, Xiao-Ping Dong
Format:	Article
Language:	English
Published:	MDPI AG 2020-09-01
Series:	Pathogens
Subjects:	genetic Creutzfeldt–Jacob disease V210I <i>PRNP</i> prion
Online Access:	https://www.mdpi.com/2076-0817/9/10/800

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