Investigating the level of Hba1c and insulin level in β-thalassemia patients
Background: β-thalassemia is an inherited blood disorder characterized by reduced or no synthesis of β globin chain, resulting in chronic anemia, so blood transfusion is required as curative therapy. Repeated blood transfusions lead to iron overload that can lead to multiple organ damage, including...
Main Authors: | Husnan Mujiburrahman, Qodri Santosa, Joko Setyono, Nendyah Roestijawati, Lantip Rujito |
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Format: | Article |
Language: | English |
Published: |
Universitas Muhammadiyah Purwokerto
2023-12-01
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Series: | Medisains |
Subjects: | |
Online Access: | https://jurnalnasional.ump.ac.id/index.php/medisains/article/view/18362 |
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