Association of GABRG2 gene polymorphisms with idiopathic generalized epilepsy in Egyptian children: a case-control study.

Eur J Med Res · 2025 · PMC12557838 · PMID 41146305

Europe PMC DOI

hedged sentences

—

closest p

—

boldest claim

The sentences

may be significantno p-value reported

Conclusions The T allele and TT genotype of the GABRG2 C588T gene were more common among patients with IGE, whereas the G allele and the GG genotype of the GABRG2 3145G>A gene may be significant predictors of ASMs resistance among IGE patients.

also in 7,550 other papers

did not reach statistical significanceno p-value reported

However, the differences between groups did not reach statistical significance, and the odds ratio for the association between the GABRG2 C588T polymorphism and the development of IGE was undetectable.

also in 75,868 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.