Disease-Modifying Effect of HBS1L-MYB in HbE/β-Thalassemia Patients in Bangladeshi Population

Disease-Modifying Effect of HBS1L-MYB in HbE/β-Thalassemia Patients in Bangladeshi Population

<b>Background:</b> Thalassemias are a group of autosomal recessive disorders and the most common inherited disease worldwide. Fetal hemoglobin (HbF) is the main oxygen carrier protein in the human fetus. Elevated HbF level is known to ameliorate the severity of HbE/β and β-thalassemia. T...

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Bibliographic Details
Main Authors: Jannatul Ferdous, Marzia Tasnim, Firdausi Qadri, Md. Ismail Hosen, Emran Kabir Chowdhury, Hossain Uddin Shekhar
Format: Article
Language:English
Published: MDPI AG 2024-11-01
Series:Thalassemia Reports
Subjects:
HbE/β-thalassemia
HBS1L-MYB
fetal hemoglobin (HbF)
hemoglobin (Hb)
Online Access:https://www.mdpi.com/2039-4365/14/4/11
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