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Updated: Jan 20, 2026
Point Mutations and Frameshift Mutations
A Novel Frameshift Mutation at Codon 2 (-T) (HBB: c.9delT) and First Report of Three New β-Globin Mutations From
Bayram Bayramov1, Gunay Aliyeva2, Chingiz Asadov2
1Genetic Resources Institute, Azerbaijan National Academy of Sciences, Baku, Azerbaijan.
Abstract:
We identified a novel mutation of β-thalassemia (β-thal) in a heterozygous carrier from Azerbaijan. Phenotypical data and molecular mechanisms of codon 2 (-T) (HBB: c.9delT) was relevant to β0-thal. Additionally, we here report two new mutations on the HBB gene, not observed previously, in the local population as well as a non causative promoter mutation -198 (A>G) (HBB: c.-248A>G).
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