Six Algerian patients with beta 0 thalassemia are presented, in addition to the two patients already reported (Godet et al., 1977). Family studies indicate that all the patients had homozygous beta thalassemia characterized by absence of beta globin chain synthesis in peripheral blood. The clinical
✦ LIBER ✦
β-Thalassemia in Algeria
✍ Scribed by D. LABIE; C. BENNANI; C. BELDJORD
- Book ID
- 119864524
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 727 KB
- Volume
- 612
- Category
- Article
- ISSN
- 0890-6564
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