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α-Globin as a molecular target in the treatment of β-thalassemia

The thalassemias, together with sickle cell anemia and its variants, are the world’s most common form of inherited anemia, and in economically undeveloped countries, they still account for tens of thousands of premature deaths every year. In developed countries, treatment of thalassemia is also stil...

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Bibliographic Details
Published in:Blood
Main Authors: Mettananda, Sachith, Gibbons, Richard J., Higgs, Douglas R.
Format: Artigo
Language:Inglês
Published: American Society of Hematology 2015
Subjects:
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4497969/
https://ncbi.nlm.nih.gov/pubmed/25869286
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2015-03-633594
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