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» Researchers unveil novel HBB gene mutation involved in β-thalassemia
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Biomarkers
Researchers unveil novel HBB gene mutation involved in β-thalassemia
Dec. 12, 2023
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It is known that heterozygous mutations in the
HBB
gene, which encodes β-globin, are the cause of inherited β-thalassemia. A new case report describes a novel frameshift mutation in the
HBB
gene leading to a dominant form of β-thalassemia.
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