NR AHAX

AU Laplanche,J.L.; Chatelain,J.C.; Thomas,S.; Launay,J.M.; Gaultier,C.; Derouesne,C.

TI Uncommon phenotype for a codon 178 mutation of the human PrP gene

QU Annals of Neurology 1992 Mar; 31(3): 345

PT letter

MH Age Factors; Case Report; Codon; Creutzfeldt-Jakob Syndrome/*genetics; Genes, Structural; Genetic Predisposition to Disease; Human; Male; Middle Age; Mutation; Pedigree; Phenotype; PrPc Proteins; Prions/*genetics; Protein Precursors/*genetics

SP englisch

PO USA

EA pdf-Datei

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