Article

Detection of −α 3.7 and _ _SEA deletions in α-globin gene in the Bangladeshi population

2024-01-03

Abstract excerpt

<h4>Background: </h4> α-thalassemia, resulting largely from deletions in the α-globin chain of hemoglobin, is one of the most common inherited blood disorders among the Asian population . The α-globin gene locus ( HBA1 and HBA2 ), located on chromosome 16p13.3, includes two highly homologous genes that produce identical α-globin protein products after translation. The most common single α-gene deletions are −α 3.7...

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Literature Corpus work: bf2abd87-d0c0-55a8-ad6b-ad43d9414fa2
DOI: 10.21203/rs.3.rs-3811767/v1

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