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Lentiviral gene transfer improves human alpha globin production for the treatment of alpha thalassemia

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Researchers at Children's Hospital of Philadelphia (CHOP) and the University of Pennsylvania Perelman School of Medicine have pioneered a new model that offers a potential platform for developing novel therapies to treat alpha thalassemia (AT), a severe blood disorder. The findings were published in the journal Blood.

Lentiviral gene transfer improves human alpha globin production for the treatment of alpha thalassemia retrieved 2 July 2024 from https://medicalxpress.com/news/2024-07-lentiviral-gene-human-alpha-globin.html

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