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

Association of GABRG2 polymorphisms with idiopathic generalized epilepsy.

Pediatric neurology - 1 Jan 2007

Chou I-Ching, Lee Cheng-Chun, Tsai Chang-Hai, Tsai Yuhsin, Wan Lei, Hsu Yu-An, Li Tsai-Chung, Tsai Fuu-Jen

Abstract excerpt

Missense mutations in the gamma2 subunit of gamma-aminobutyric acid (GABA) receptor gene have recently been described in families with idiopathic generalized epilepsies. This study aimed to evaluate whether polymorphisms of the gamma2 subunit of the GABA receptor gene are associated with idiopathic generalized epilepsies. A total of 77 children with idiopathic generalized epilepsies and 83 normal control subjects...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Child
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 5

Share to Epilepsy, Generalized

Share to Gene Frequency

Share to Receptors, GABA-A

Share to Receptors, GABA-B

Source

Identifiers

PMID: 17162195
DOI: 10.1016/j.pediatrneurol.2006.09.011

Genes

GABRG2

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

Association of GABRG2 polymorphisms with idiopathic generalized epilepsy.PMID 17162195Read ↗

Association of rs211037 GABRG2 gene polymorphism with susceptibility to idiopathic generalized epilepsy.Semantic proximity Read ↗

The genetic variant "C588T" of GABARG2 is linked to childhood idiopathic generalized epilepsy and resistance to antiepileptic drugs.Semantic proximity Read ↗

Contribution of GABRG2 Polymorphisms to Risk of Epilepsy and Febrile Seizure: a Multicenter Cohort Study and Meta-analysis.Semantic proximity Read ↗

Analysis of GABRG2 C588T polymorphism in genetic epilepsy and evaluation of GABRG2 in drug treatment.Semantic proximity Read ↗

GABRG2 rs211037 polymorphism and epilepsy: a systematic review and meta-analysis.Semantic proximity Read ↗

First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene.Semantic proximity Read ↗

Molecular Pathogenic Basis for GABRG2 Mutations Associated With a Spectrum of Epilepsy Syndromes, From Generalized Absence Epilepsy to Dravet Syndrome.Semantic proximity Read ↗

Association analysis of gamma 2 subunit of gamma- aminobutyric acid type A receptor polymorphisms with febrile seizures.Semantic proximity Read ↗

The GABAA receptor γ2 subunit (R43Q) mutation in febrile seizures.Semantic proximity Read ↗

Identification of SNPs in human gamma aminobutyric acid A receptor gamma2 gene.Semantic proximity Read ↗

Mutational analysis of GABRG2 in a Japanese cohort with childhood epilepsiesSemantic proximity Read ↗

GABRA1 and GABRA6 gene mutations in idiopathic generalized epilepsy patients.Semantic proximity Read ↗

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