A REVIEW: THE ROLE OF SNPS IN HBB, BCL11A, HBS1L-MYB, AND MIRNA NETWORKS IN BETA-THALASSEMIA: INSIGHTS FROM IRAQI AND ASIAN POPULATIONS
Haider Qassim Raheem; Haider Turky Mousa AL-Mousawi; Yasir Haider Al-Mawlah; Humam Fadel Al-Sultani; Hussein Fadil I brahim; Shatha Ruaidh Shather; Hawraa Majid Hassan; Sajjad Haider Jasim
Objective: Beta-thalassemia is a genetically heterogeneous blood disorder marked by impaired hemoglobin synthesis, resulting in chronic anemia, multi-organ complications, and changing clinical severity. This review analyzes the essential functions...