A SPONTANEOUS DELETION OF β33/34 Val IN EXON 2 OF THE β GLOBIN GENE (Hb KOREA) PRODUCES THE PHENOTYPE OF DOMINANT β THALASSAEMIA
- 1 August 1991
- journal article
- case report
- Published by Wiley in British Journal of Haematology
- Vol. 78 (4) , 581-582
- https://doi.org/10.1111/j.1365-2141.1991.tb04499.x
Abstract
No abstract availableKeywords
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- Molecular basis for dominantly inherited inclusion body beta-thalassemia.Proceedings of the National Academy of Sciences, 1990
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- Frameshift Mutations and the Genetic CodeCold Spring Harbor Symposia on Quantitative Biology, 1966