Characterization of Anchorless Human PrP With Q227X Stop Mutation Linked to Gerstmann-Sträussler-Scheinker Syndrome In Vivo and In Vitro.
Mol Neurobiol
; 58(1): 21-33, 2021 Jan.
Article
in En
| MEDLINE
| ID: mdl-32889654
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Prions
/
Gerstmann-Straussler-Scheinker Disease
/
Codon, Nonsense
Limits:
Adult
/
Animals
/
Female
/
Humans
Language:
En
Journal:
Mol Neurobiol
Journal subject:
BIOLOGIA MOLECULAR
/
NEUROLOGIA
Year:
2021
Document type:
Article