Genetic Variants of β-Thalassemia and Hemoglobin E β-Thalassemia: A Mutation Profiling Study in the Bangladeshi Population

Background: β-Thalassemia and Hb E β-Thalassemia are among the most prevalent genetic disorders in Bangladesh. Haemoglobin E is also one of the most common hemoglobinopathies worldwide, particularly among individuals of Southeast Asian, Northeast Indian, Sri Lankan, and Bangladeshi descent. It is c...

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Κύριοι συγγραφείς:	Salma Sadiya, Md. Abdul Aziz, Rowshon Zahan Luna, Kaosarul Alam, Md. Masud Rana
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	Haematology Society of Bangladesh 2026-01-01
Σειρά:	Haematology Journal of Bangladesh
Θέματα:	β-thalassemia haemoglobinopathy carrier mutations ARMS PCR Sanger sequencing
Διαθέσιμο Online:	https://journal.hematologybd.org/index.php/haematoljbd/article/view/161
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