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Genetic Mutation of Hb E/beta Thalassemia Patient in Bangladesh and Its Relation With Clinical Severity

2021-09-29

Abstract excerpt

<title>Abstract</title> <p><bold>Background: </bold>Hemoglobin E/β-thalassemia is a common inherited hemoglobin disorder among South Asian countries. The phenotypically diverse presentation of the disease is often attributed to coinheritance of β-globin (<italic>HBB</italic>) gene mutations. The current study described the phenotype and genetic basis of Hb E/β-thalassemia patients and assessed its relation with c...

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Literature Corpus work
f0344eef-bcc8-5d9a-a657-fe7b3f2008c1
DOI
10.21203/rs.3.rs-927268/v1
Open publication

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Genetic Mutation of Hb E/beta Thalassemia Patient in Bangladesh and Its Relation With Clinical SeverityDOI 10.21203/rs.3.rs-927268/v1
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