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 Creutzfeldt–Jacob di...
I tiakina i:
| Ngā kaituhi matua: | , , , , , , , , |
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| Hōputu: | Artigo |
| Reo: | Inglês |
| I whakaputaina: |
MDPI AG
2020-09-01
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| Rangatū: | Pathogens |
| Ngā marau: | |
| Urunga tuihono: | https://www.mdpi.com/2076-0817/9/10/800 |
| Ngā Tūtohu: |
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
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