Heterozygous β-thalassemia with thalasse
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Gasperini, D.; Perseu, L.; Melis, M.A.; Maccioni, L.; Sollaino, M.C.; Paglietti,
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Article
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1998
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John Wiley and Sons
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English
⚖ 54 KB
In this study we investigated the molecular bases of the beta-thalassemia intermedia phenotype in six patients belonging to two unrelated families of Sardinian descent. Sequence analysis of the beta globin gene from these patients detected, as the sole abnormality, the heterozygosity for the codon 3