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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
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Prion Diseases / PrPSc Proteins / Mutation Limits: Humans Language: En Journal: Ann Neurol Year: 2004 Document type: Article