Mutation at codon 210 (V210I) of the prion protein gene in a North African patient with Creutzfeldt-Jakob disease.

Mouillet-Richard, S; Teil, C; Lenne, M; Hugon, S; Taleb, O; Laplanche, J L

Mouillet-Richard, S; Teil, C; Lenne, M; Hugon, S; Taleb, O; Laplanche, J L.

Affiliation

Mouillet-Richard S; Centre de Recherche C. Bernard, IFR 6, Service de Biochimie (Pr. J. -M. Launay), Hôpital Lariboisière, 2 rue A. Paré, 75475, Paris, France.

J Neurol Sci ; 168(2): 141-4, 1999 Oct 15.

Article in En | MEDLINE | ID: mdl-10526198

Subject(s)

Amyloid/genetics; Creutzfeldt-Jakob Syndrome/genetics; Protein Precursors/genetics; Amino Acid Substitution; DNA Mutational Analysis; Electroencephalography; Genetic Carrier Screening; Humans; Male; Middle Aged; Pedigree; Point Mutation; Polymorphism, Genetic; Prion Proteins; Prions

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Collection: 01-internacional Database: MEDLINE Main subject: Protein Precursors / Creutzfeldt-Jakob Syndrome / Amyloid Limits: Humans / Male / Middle aged Language: En Journal: J Neurol Sci Year: 1999 Type: Article Affiliation country: France

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