Impact of MTHFR Gene Polymorphisms C677T and A1298C on Congenital Atrial Septal Defect Risk in an Iranian Cohort
Our findings suggest that <i>MTHFR</i> rs1801133 and rs1801131 variants may potentially affect the onset of ASD.
Authors
- Mohsen Taheri (ORCID: https://orcid.org/0000-0002-1110-4417)
- Saeedeh Yaghoubi (ORCID: https://orcid.org/0000-0003-3739-1749)
- Gholamreza Bahari (ORCID: https://orcid.org/0000-0003-2531-4236)
- Noor Mohammad Noori (ORCID: https://orcid.org/0000-0002-0732-6412)
- Ali Aghighi
Institutions
- Zahedan University of Medical Sciences (IR)
Publication Details
- Journal
- Reports of Biochemistry and Molecular Biology
- Published
- 2024-11-01
- DOI
- https://doi.org/10.61186/rbmb.13.3.377
- Primary Topic
- Congenital Heart Disease Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Zahedan University of Medical Sciences