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. 2024 Mar;91(3):309.
doi: 10.1007/s12098-023-04825-0. Epub 2023 Sep 14.

Compound Heterozygous for Asian Inversion Deletion Gγ (Aγδβ)0 and IVS1-5 (G→C) β Thalassemia Mutation in a Transfusion-Dependent Patient

Sujata Dixit  1   2 , Arundhuti Das  1 , Swati Sudeshna Panigrahi  1 , Palash Das  3 , Priyanka Samal  4 , Madhusmita Bal  1 , Sanghamitra Pati  1 , Manoranjan Ranjit  5
Affiliations

Compound Heterozygous for Asian Inversion Deletion Gγ (Aγδβ)0 and IVS1-5 (G→C) β Thalassemia Mutation in a Transfusion-Dependent Patient

Sujata Dixit et al. Indian J Pediatr. 2024 Mar.
No abstract available

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References

    1. Craig JE, Barnetson RA, Prior J, Raven JL, Thein SL. Rapid detection of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification. Blood. 1994;83:1673–82. - DOI - PubMed
    1. Varawalla NY, Old JM, Sarkar R, Venkatesan R, Weatherall DJ. The spectrum of beta- thalassemia mutation on the indian subcontinent: the basis of prenatal diagnosis. Br J Haematol. 1991;78:242–7. - DOI - PubMed
    1. Dehury S, Purohit P, Meher S, Das K, Patel S. Compound heterozygous state of β-thalassemia with IVS1-5 (G→C) mutation and indian deletion-inversion Gγ(Aγδβ)(o)-thalassemia in eastern India. Rev Bras Hematol Hemoter. 2015;37:202–6. - DOI - PubMed - PMC

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