Article
Beta-thalassemia, HB S-beta-thalassemia and sickle cell anemia among Tunisians.
Hemoglobin - 1 Jan 1991
Fattoum S, Guemira F, Oner C, Oner R, Li H W, Kutlar F, Huisman T H
Abstract excerpt
We analyzed the mutations present in 19 patients with beta-thalassemia major, in 11 patients with Hb S-beta-thalassemia, and the beta S haplotypes of 34 patients with sickle cell anemia. The study included 84 relatives. Dot-blot analysis of amplified DNA with various specific oligonucleotide probes identified 11 different known beta-thalassemia mutations and frameshifts; a new frameshift at codons 25/26 (+T) was...
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