NF-κB pathway variants in Iranian patients with inborn errors of immunity
This study identifies novel IEI cases associated with NF-κB pathway defects. Further comprehensive evaluation and functional analysis of these mutations are warranted to confirm their impact on disease manifestation.
Authors
- Nazanin Fathi (ORCID: https://orcid.org/0000-0002-9562-9623)
- Arash Kalantari
- Samaneh Delavari (ORCID: https://orcid.org/0000-0003-0122-0657)
- Sareh Sadat Ebrahimi
- Reza Yazdani
- Nima Rezaei (ORCID: https://orcid.org/0000-0002-3836-1827)
- Hassan Abolhassani (ORCID: https://orcid.org/0000-0002-4838-0407)
- Seyed Alireza Mahdaviani (ORCID: https://orcid.org/0000-0001-6224-4797)
- Tannaz Moeini Shad (ORCID: https://orcid.org/0000-0002-9958-3191)
- Nasrin Beniafard
- Fereshte Salami
Institutions
- Shahid Sadoughi University of Medical Sciences and Health Services (IR)
- Kerman University of Medical Sciences (IR)
- Karolinska Institutet (SE)
- Universal Scientific Education and Research Network (IR)
- Shahid Beheshti University of Medical Sciences (IR)
- Tehran University of Medical Sciences (IR)
Publication Details
- Journal
- Expert Review of Clinical Immunology
- Published
- 2025-05-04
- DOI
- https://doi.org/10.1080/1744666x.2025.2500608
- Primary Topic
- Immunodeficiency and Autoimmune Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Tehran University of Medical Sciences and Health Services