Heterogeneity in β0thalassemia from Alge
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Mériem Belhani; F. Morlé; P. Colonna; Jacqueline Godet
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Article
📅
1980
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Springer
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English
⚖ 537 KB
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