A new frameshift mutation, insertion of ATCT, at codon 48 in the β-globin gene causes β-thalassemia in an Indian proband
- 1 January 1994
- journal article
- mutation in-brief
- Published by Hindawi Limited in Human Mutation
- Vol. 3 (4) , 397-398
- https://doi.org/10.1002/humu.1380030413
Abstract
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This publication has 3 references indexed in Scilit:
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- Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean beta-thalassemia mutations by covalent reverse dot-blot analysis: application to prenatal diagnosis in SicilyBlood, 1993
- The spectrum of β‐thalassaemia mutations on the Indian subcontinent: the basis for prenatal diagnosisBritish Journal of Haematology, 1991