Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Molecular genetics in Creutzfeldt-Jakob disease].

Rinsho shinkeigaku = Clinical neurology - 1 Dec 1994

Kitamoto T

Abstract excerpt

Recent molecular genetic studies revealed that human prion protein (PrP) gene has a large repertoire of polymorphisms and mutations. Each variant PrP seems to correspond to the distinct type of prion diseases. We report herein that it is useful to classify prion diseases into Creutzfeldt-Jakob disease (CJD) type or Gerstmann-Sträussler syndrome (GSS) type, based on the distribution of PrP in the central nervous...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Creutzfeldt-Jakob Syndrome
Share to GSS gene
Share to Gerstmann-Straussler-Scheinker Disease

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

Share to Mutation

Share to Polymorphism, Genetic

Share to Prions

Source

Identifiers

PMID: 7774117

Genes

GSS

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Molecular genetics in Creutzfeldt-Jakob disease].PMID 7774117Read ↗

Genetic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

[Prion diseases, update].Semantic proximity Read ↗

[A trend of molecular genetics on prion diseases and prion protein].Semantic proximity Read ↗

Systematic Review of Clinical and Pathophysiological Features of Genetic Creutzfeldt-Jakob Disease Caused by a Val-to-Ile Mutation at Codon 180 in the Prion Protein Gene.Semantic proximity Read ↗

[Creutzfeldt-Jakob Disease].Semantic proximity Read ↗

Prion disease genetics.Semantic proximity Read ↗

The prion diseases.Semantic proximity Read ↗

[Clinicopathological characteristics of Creutzfeldt-Jakob disease with a PrP V180I mutation and M129V polymorphism on different alleles].Semantic proximity Read ↗

[Clinical characteristics and laboratory findings in prion diseases].Semantic proximity Read ↗

[Creutzfeldt-Jakob encephalopathy with mutation E200K. Report of a "sporadic" case].Semantic proximity Read ↗

Genetic studies in human prion diseases.Semantic proximity Read ↗

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

⌁Select a neighboring publication to make it the new centre.