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Defective Translational Control in the β-Thalassemia of Ferrara

  • Francesco Conconi
  • Laura del Senno
Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 44)

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.

Keywords

Tube Number Label Amino Acid FEBS Letter Cellulose Column Globin mRNA 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Plenum Press, New York 1974

Authors and Affiliations

  • Francesco Conconi
    • 1
  • Laura del Senno
    • 1
  1. 1.Centro di Studi Biochimici sul Morbo di Cooley Cassa di Risparmio di Ferrara c/o Instituto di ChimicaBiologica dell’Università degli Studi di FerraraFerraraItaly

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