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Article

Valine homozygous 129 PrP genotype in a French growth-hormone-related Creutzfeldt-Jakob disease patient.

Neurology - 1 Feb 1993

Labauge P, Pagès M, Blard J M, Chatelain J, Laplanche J L

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 8437720
DOI: 10.1212/wnl.43.2.447

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Valine homozygous 129 PrP genotype in a French growth-hormone-related Creutzfeldt-Jakob disease patient.PMID 8437720Read ↗

Creutzfeldt-Jakob disease after pituitary-derived human growth hormone therapy: two cases with valine 129 homozygous genotype.Semantic proximity Read ↗

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Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation.Semantic proximity Read ↗

Molecular characterisation and diagnosis of Hb J-Taichung (129[H7]Ala-->Asp) in a Taiwanese family subject.Semantic proximity Read ↗

A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease.Semantic proximity Read ↗

Creutzfeldt-Jakob disease with the V203I mutation and M129V polymorphism of the prion protein gene (PRNP) and a 17 kDa prion protein fragment.Semantic proximity Read ↗

Genetic analysis of Creutzfeldt-Jakob disease and related disorders.Semantic proximity Read ↗

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Creutzfeldt-Jakob disease in a Chinese patient with a novel seven extra-repeat insertion in PRNP.Semantic proximity Read ↗

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