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    Globin gene deletion in HPFH, δ°β° thalassaemia and Hb Lepore disease

    THE thalassaemias are a group of inherited disorders characterised by the defective production of either α (α thalassaemias) or non-α (β and δ°β° thalassaemias) globin chains of haemoglobins (Hb)1. In β thalassae...

    S. OTTOLENGHI, B. GIGLIONI, P. COMI, A. M. GIANNI, E. POLLI, C. T. A. ACQUAYE… in Nature (1979)