Abstract
β-Thalassemia is a genetically determined anemia of man, characterized by a decreased synthesis of β-globin (and consequently of hemoglobin A) and a relative excess of α-globin synthesis.
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Conconi, F., del Senno, L. (1974). Defective Translational Control in the β-Thalassemia of Ferrara . In: Kohn, A., Shatkay, A. (eds) Control of Gene Expression. Advances in Experimental Medicine and Biology, vol 44. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-3246-6_12
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DOI: https://doi.org/10.1007/978-1-4684-3246-6_12
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