HB Shelby [α2β2131(H9)GLN→LYS]-β°-Thalassemia [Codon 15 (TGG→TGA)] Identified by DNA Sequencing
- 1 January 1992
- journal article
- case report
- Published by Taylor & Francis in Hemoglobin
- Vol. 16 (5) , 417-419
- https://doi.org/10.3109/03630269209005694
Abstract
(1992). HB Shelby [α2β2131(H9)GLN→LYS]-β°-Thalassemia [Codon 15 (TGG→TGA)] Identified by DNA Sequencing. Hemoglobin: Vol. 16, No. 5, pp. 417-419. doi: 10.3109/03630269209005694Keywords
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- Hb Leslie, an unstable hemoglobin due to deletion of glutaminyl residue beta 131 (H9) occurring in association with beta0-thalassemia, HbC, and HbSBlood, 1976