Molecular spectrum and carrier frequency of deletional hereditary persistence of fetal hemoglobin and delta-beta thalassemia in Malaysia
This study provides crucial data on the molecular spectrum of HPFH and δβ thalassemia in Malaysia, contributing to improved diagnostic strategies and genetic counselling. Future research should explore additional genetic variants to enhance national thalassemia prevention programs.
Authors
- Mei I Lai (ORCID: https://orcid.org/0000-0002-5992-9397)
- Faidatul Syazlin Abdul Hamid (ORCID: https://orcid.org/0009-0006-8471-7712)
- Norafiza Mohd Yasin (ORCID: https://orcid.org/0000-0003-4202-2438)
- Ezalia Esa (ORCID: https://orcid.org/0000-0001-8699-1017)
- Yuslina Mat Yusoff (ORCID: https://orcid.org/0009-0001-8534-0551)
- Ermi Neiza Mohd Sahid (ORCID: https://orcid.org/0009-0008-7117-6624)
- Sabariah Md Noor (ORCID: https://orcid.org/0000-0002-2292-5149)
- Samsol Kamal Mohd Bahari
Institutions
- Universiti Putra Malaysia (MY)
- Management and Science University (MY)
- Institute of Clinical Research (GB)
- National Institutes of Biotechnology Malaysia (MY)
Publication Details
- Journal
- Blood Research
- Published
- 2025-09-29
- DOI
- https://doi.org/10.1007/s44313-025-00100-7
- Primary Topic
- Hemoglobinopathies and Related Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00