Striking PrPsc heterogeneity in inherited prion diseases with the D178N mutation.
Ann Neurol
; 56(6): 909-10; author reply 910-1, 2004 Dec.
Article
in En
| MEDLINE
| ID: mdl-15562434
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Prion Diseases
/
PrPSc Proteins
/
Mutation
Limits:
Humans
Language:
En
Journal:
Ann Neurol
Year:
2004
Document type:
Article