Compound Heterozygosity for β+-Thalassemia [-31 (A→G)] and a New Variant with Low Oxygen Affinity, Hb Sagami [β139(H17)Asn→Thr]
- 1 January 1999
- journal article
- case report
- Published by Taylor & Francis in Hemoglobin
- Vol. 23 (3) , 267-271
- https://doi.org/10.3109/03630269909005708
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
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- Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene clusterNature, 1982