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Article

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

Journal of neurology, neurosurgery, and psychiatry - 1 Feb 2007

Wang X F, Guo Y J, Zhang B Y, Zhao W Q, Gao J M, Wan Y Z, Li F, Han J, Wang D X, Dong X P

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Identifiers

PMID: 17229753
DOI: 10.1136/jnnp.2006.09433
PMCID: PMC2077666

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.

Research trail→

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Creutzfeldt-Jakob disease in a Chinese patient with a novel seven extra-repeat insertion in PRNP.PMID 17229753Read ↗

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

De novo seven extra repeat expanded mutation in the PRNP gene in an Italian patient with early onset dementia.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 ↗

Polymorphisms of the PRNP gene in Chinese populations and the identification of a novel insertion mutation.Semantic proximity Read ↗

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene.Semantic proximity Read ↗

Rare V180I mutation in PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease.Semantic proximity Read ↗

Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation.Semantic proximity Read ↗

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

A Chinese Creutzfeldt-Jakob disease patient with E196K mutation in PRNP.Semantic proximity Read ↗

A novel duplication/insertion mutation of NEFL in a patient with Charcot-Marie-Tooth disease.Semantic proximity Read ↗

Rare E196A mutation in PRNP gene of 3 Chinese patients with Creutzfeldt-Jacob disease.Semantic proximity Read ↗

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

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