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 EIF4G1 in Parkinson's disease among Asians.

Neurobiology of aging - 1 Apr 2013

Zhao Yi, Ho Patrick, Prakash Kumar-M, Foo Jia-Nee, Liu Jian-Jun, Au Wing-Lok, Tan Louis C, Tan Eng-King

Abstract excerpt

Sequence analysis of all the exons of EIF4G1 in 96 Asian patients with Parkinson's disease (PD) did not reveal any pathogenic mutations. A novel coding variant (Pro693Ser) in exon 15 (position 2077) was detected in one PD patient but not in 539 control subjects. Analysis of a coding polymorphic variant (rs2178403) in 1330 subjects revealed similar frequency between control subjects (0.638) and PD patients...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Eukaryotic Initiation Factor-4G

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Markers

Share to Parkinson Disease

Share to Prevalence

Share to Risk Factors

Share to United Kingdom

Source

Identifiers

PMID: 23092605
DOI: 10.1016/j.neurobiolaging.2012.09.003

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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 EIF4G1 in Parkinson's disease among Asians.PMID 23092605Read ↗

Analysis of EIF4G1 in ethnic Chinese.Semantic proximity Read ↗

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

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

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

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

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

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

The EIF4G1 gene and Parkinson's disease.Semantic proximity Read ↗

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

Association analysis of EIF4G1 and Parkinson disease in Xinjiang Uygur and Han nationality.Semantic proximity Read ↗

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

Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore.Semantic proximity Read ↗

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