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Article

[Genetic markers in four Chilean families with familial Creutzfeldt-Jakob disease].

Revista medica de Chile - 1 Sept 2006

Cartier R Luis, Fernández O Jorge, Ramírez V Eugenio

Abstract excerpt

BACKGROUND: Creutzfeldt-Jakob disease (CJD) is a form of transmissible spongiform encephalopathy, in which a prion protein (PrP Sc) accumulates in the brain of affected individuals. Chile has a prevalence of CJD that is more than twice than in the rest of the world and has the highest rate of familial forms. These later forms are associated with the heterozygocity of codon 200 of PrP protein gene. AIM: To search...

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Identifiers

PMID: 17171212
DOI: 10.4067/s0034-98872006000900005

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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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[Genetic markers in four Chilean families with familial Creutzfeldt-Jakob disease].PMID 17171212Read ↗

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Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease.Semantic proximity Read ↗

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