Associated gene polymorphism (ABCG2) and drug-resistant in Patients with epilepsy
Conclusions: Overall, the study found that the ABCG2 C>T (rs2231137) polymorphism is associated with an increased risk of epilepsy. Specifically, the patient group was more likely to have the heterozygous genotype CT, with the allele C, compared to the control group.
Authors
- Maysaa Ali Abdul Khaleq (ORCID: https://orcid.org/0000-0003-3548-7835)
- Ahmed Hamza Ajmi
- Ghada Ibrahim
Institutions
- Zagazig University (EG)
- Baghdad Medical City (IQ)
- University of Al Maarif (IQ)
- Ministry of Health (IQ)
Publication Details
- Journal
- Wiadomości Lekarskie
- Published
- 2025-02-28
- DOI
- https://doi.org/10.36740/wlek/200736
- Primary Topic
- Epilepsy research and treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00