Towards the genetic treatment of β-thalassemia: new disease models, new vectors, new cells
Haematologica 2008 93: 325-330.
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The transfer of a regulated globin gene in autologous hematopoietic stem cells is an attractive therapeutic approach to β-thalassemia, since, in principle, it is applicable to all patients. This commentary reviews recent advances in animal models, globin vector design and stem cell isolation. See related article on page 356.