Impact of Xmn1 polymorphism on hydroxyurea therapy in children with HbE-β non-transfusion dependent thalassemia: a cohort study
The T allele of the Xmn1 polymorphism had a favorable effect on the efficacy of hydroxyurea in patients with HbE-β-NTDT.
Authors
- S. K. Roy (ORCID: https://orcid.org/0000-0003-0135-5738)
- Atanu Kumar Dutta (ORCID: https://orcid.org/0000-0002-8413-3454)
- Paramita Bhattacharya (ORCID: https://orcid.org/0000-0003-3871-9400)
- Mrinal Kanti Das (ORCID: https://orcid.org/0000-0003-0840-3632)
Institutions
- P. D. Hinduja Hospital and Medical Research Centre (IN)
- National Institute of Biomedical Genomics (IN)
- All India Institute of Medical Sciences (IN)
- Medical College and Hospital, Kolkata (IN)
- University of Kalyani (IN)
Publication Details
- Journal
- Clinical and Experimental Pediatrics
- Published
- 2025-02-03
- DOI
- https://doi.org/10.3345/cep.2024.01284
- Primary Topic
- Hemoglobinopathies and Related Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00