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Article

Creutzfeldt-Jakob disease with a novel insertion and codon 219 Lys/Lys polymorphism in PRNP.

Neurology - 23 Nov 2004

Nishida Y, Sodeyama N, Toru Y, Toru S, Kitamoto T, Mizusawa H

Abstract excerpt

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15557533
DOI: 10.1212/01.wnl.0000144196.43430.e1

Genes

PRNP

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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Creutzfeldt-Jakob disease with a novel insertion and codon 219 Lys/Lys polymorphism in PRNP.PMID 15557533Read ↗

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

A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene.Semantic proximity Read ↗

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

Probable genetic Creutzfeldt-Jakob Disease with rare E196K mutation.Semantic proximity Read ↗

Brain 18F-FDG PET/CT findings in a case of genetic Creutzfeldt-Jakob disease due to V203I heterozygous mutation in the PRNP gene.Semantic proximity Read ↗

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

Codon 219 in Creutzfeldt-Jakob disease in Poland.Semantic proximity Read ↗

A novel mutation I215V in the PRNP gene associated with Creutzfeldt-Jakob and Alzheimer's diseases in three patients with divergent clinical phenotypes.Semantic proximity Read ↗

Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families.Semantic proximity Read ↗

Rare genetic E196A mutation in a patient with Creutzfeldt-Jakob disease: a case report and literature.Semantic proximity Read ↗

Mutation of the PRNP gene at codon 211 in familial Creutzfeldt-Jakob disease.Semantic proximity Read ↗

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