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

Study of the genetic variability in a Parkinson's Disease gene: EIF4G1.

Neuroscience letters - 14 Jun 2012

Tucci Arianna, Charlesworth Gavin, Sheerin Una-Marie, Plagnol Vincent, Wood Nicholas W, Hardy John

Abstract excerpt

Chartier-Harlin and colleagues [2] recently reported mutations in the eukaryotic translation initiation factor 4-gamma (EIF4G1) gene in families with parkinsonism. Large-scale screening found two mutations (p.R1205H and p.A502V) only in affected individuals, although their relative frequency was very low. The aim of this study was to investigate EIF4G1 parkinsonism-related variants in two separate cohorts and...

Read the complete abstract on PubMed

Topics

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

Share to Africa South of the Sahara
Share to Cohort Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Eukaryotic Initiation Factor-4G

Share to Parkinson Disease

Share to Polymorphism, Genetic

Share to Sequence Analysis

Share to White People

Source

Open in PubMed Open full text

Identifiers

PMID: 22561553
DOI: 10.1016/j.neulet.2012.04.033
PMCID: PMC3769807

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Study of the genetic variability in a Parkinson's Disease gene: EIF4G1.PMID 22561553Read ↗

Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's disease.Semantic proximity Read ↗

EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?Semantic proximity Read ↗

EIF4G1 mutations do not cause Parkinson's disease.Semantic proximity Read ↗

Analysis of EIF4G1 in ethnic Chinese.Semantic proximity Read ↗

Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease.Semantic proximity Read ↗

Translation initiator EIF4G1 mutations in familial Parkinson disease.Semantic proximity Read ↗

Analysis of EIF4G1 in Parkinson's disease among Asians.Semantic proximity Read ↗

EIF4G1 Ala502Val and Arg1205His variants in Chinese patients with Parkinson diseaseSemantic proximity Read ↗

Sequence variants in eukaryotic translation initiation factor 4-gamma (eIF4G1) are associated with Lewy body dementia.Semantic proximity Read ↗

ATP13A2 variability in Parkinson disease.Semantic proximity Read ↗

Eukaryotic translation initiation factor 4-γ, 1 gene mutations are rare in Parkinson's disease among Taiwanese.Semantic proximity Read ↗

EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population.Semantic proximity Read ↗

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