Rare pathogenic NR2F2 (COUP-TFII) variants as potential etiological causes in pediatric patients with congenital heart diseases (CHDs)
The results we obtained not only validate the correlation between NR2F2 mutations and CHDs but also have significant potential for guiding new preventive and therapeutic strategies. This could contribute to the advancement of medical interventions in the fields of cardiology and genetics.
Authors
- Mehdi Hadadzadeh (ORCID: https://orcid.org/0000-0003-0066-7369)
- Wasat Mansoor
- Mohammad Heidari (ORCID: https://orcid.org/0000-0002-3328-4746)
- Marzieh Araghi
- Fateme Darchin Tabrizi (ORCID: https://orcid.org/0000-0001-7856-1527)
- Mehri Khatami (ORCID: https://orcid.org/0000-0002-5840-5399)
Institutions
- Yazd University (IR)
- Shahid Sadoughi University of Medical Sciences and Health Services (IR)
Publication Details
- Journal
- Hellenic Journal of Cardiology
- Published
- 2025-02-01
- DOI
- https://doi.org/10.1016/j.hjc.2025.02.005
- Citations
- 1
- Primary Topic
- Congenital Heart Disease Studies
- Type
- article
- Field-Weighted Citation Impact
- 1.35