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...
| Main Authors: | , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2020-09-01
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| Series: | Pathogens |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2076-0817/9/10/800 |