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

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

Neuropathology and applied neurobiology - 1 Oct 2010

Jeong B-H, Jeon Y-C, Lee Y-J, Cho H-J, Park S-J, Chung D-I, Kim J, Kim S H, Kim H-T, Choi E-K, Choi K-C, Carp R I, Kim Y-S

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Blotting, Western
Share to Brain
Share to Creutzfeldt-Jakob Syndrome

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

Share to Fatal Outcome

Share to Polymerase Chain Reaction

Share to Prion Proteins

Share to Prions

Share to PrPSc Proteins

Source

Identifiers

PMID: 20497338
DOI: 10.1111/j.1365-2990.2010.01094.x

Genes

PRNP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 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

Creutzfeldt-Jakob disease with the V203I mutation and M129V polymorphism of the prion protein gene (PRNP) and a 17 kDa prion protein fragment.PMID 20497338Read ↗

Genetic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

R208H-129VV haplotype in the prion protein gene: phenotype and neuroimaging of a patient with genetic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

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

Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment.Semantic proximity Read ↗

Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype.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 ↗

Prion disease genetics.Semantic proximity Read ↗

Codon 129 polymorphism of the PRNP gene in normal Polish population and in Creutzfeldt-Jakob disease, and the search for new mutations in PRNP gene.Semantic proximity Read ↗

Genetic prion disease with codon 196 PRNP mutation: clinical and pathological findings.Semantic proximity Read ↗

Creutzfeldt-Jakob disease associated with a V203I homozygous mutation in the prion protein gene.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 ↗

Genetic studies in human prion diseases.Semantic proximity Read ↗

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