Compound Heterozygous for Asian Inversion Deletion Gγ (Aγδβ)0 and IVS1-5 (G→C) β Thalassemia Mutation in a Transfusion-Dependent Patient
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s12098-023-04825-0.pdf
Reference3 articles.
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.
2. 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.
3. 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.
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