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Article

Identification in Israel of 2 Jewish Creutzfeld-Jakob disease patients with a 178 mutation at their PrP gene.

Acta neurologica Scandinavica - 1 Mar 1998

Rosenmann H, Vardi J, Finkelstein Y, Chapman J, Gabizon R

Abstract excerpt

Among the dozen known mutations in the PrP gene which segregate with the inherited prion diseases, only 2 mutations have been described in Israel so far: the codon 200 mutation in Creutzfeldt-Jakob disease (CJD) affected Libyan Jews, and the codon 102 mutation in 1 Jewish Gerstmann-Straussler-Scheinker (GSS) affected pedigree of German origin. We report here 2 unrelated CJD178 cases affected by a unique...

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Identifiers

PMID: 9531435
DOI: 10.1111/j.1600-0404.1998.tb00634.x

Genes

GSS

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Identification in Israel of 2 Jewish Creutzfeld-Jakob disease patients with a 178 mutation at their PrP gene.PMID 9531435Read ↗

Genetics and biochemistry of Creutzfeldt-Jakob disease in Libyan Jews.Semantic proximity Read ↗

Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation.Semantic proximity Read ↗

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Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene.Semantic proximity Read ↗

A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease.Semantic proximity Read ↗

Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation.Semantic proximity Read ↗

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Fatal familial insomnia with a mutation at codon 178 of the prion protein gene: first report from Japan.Semantic proximity Read ↗

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