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

[Analysis of GBA mutations in patients with Parkinson's disease in the Krasnoyarsk region].

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova - 1 Jan 2023

Subbotina T N, Abramov V G, Shaleva A A, Vereschagina S V, Pokhabov D V

Abstract excerpt

OBJECTIVE: To analyze mutations and polymorphisms in exons 2, 7, 8, 9, 10 and 11 of the glucocerebrosidase (GBA) gene in patients of the Krasnoyarsk region diagnosed with Parkinson's disease (PD). MATERIAL AND METHODS: Seventy-five patients with sporadic and familial forms of PD were examined. Genomic DNA was isolated from the whole blood of patients. The above mentioned exons of GBA were analyzed using Sanger...

Read the complete abstract on PubMed

Topics

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

Share to Genetic Predisposition to Disease
Share to Glucosylceramidase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Parkinson Disease

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 37084373
DOI: 10.17116/jnevro2023123041103

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Analysis of GBA mutations in patients with Parkinson's disease in the Krasnoyarsk region].PMID 37084373Read ↗

Glucocerebrosidase mutations in a Serbian Parkinson's disease population.Semantic proximity Read ↗

Glucocerebrosidase gene mutations are associated with Parkinson's disease in RussiaSemantic proximity Read ↗

Mutations in glucocerebrosidase are a major genetic risk factor for Parkinson's disease and increase susceptibility to dementia in a Flanders-Belgian cohort.Semantic proximity Read ↗

Glucocerebrosidase mutations in Thai patients with Parkinson's disease.Semantic proximity Read ↗

Mutations in the glucocerebrosidase gene are responsible for Chinese patients with Parkinson's disease.Semantic proximity Read ↗

Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Greece.Semantic proximity Read ↗

[The clinical features of Parkinson's disease in patients with mutations and polymorphic variants of GBA gene].Semantic proximity Read ↗

Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease.Semantic proximity Read ↗

Mutations in the glucocerebrosidase gene are common in patients with Parkinson's disease from Eastern Canada.Semantic proximity Read ↗

[A PARK8 form of Parkinson's disease: a mutational analysis of the LRRK2 gene in Russian population].Semantic proximity Read ↗

[Distribution of mutations of acid beta-D-glucosidase gene (GBA) among 68 Russian patients with Gaucher's disease].Semantic proximity Read ↗

Glucocerebrosidase L444P mutation confers genetic risk for Parkinson's disease in central China.Semantic proximity Read ↗

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