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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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Detalhes bibliográficos
Publicado no:Blood
Main Authors: Mettananda, Sachith, Gibbons, Richard J., Higgs, Douglas R.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2015
Assuntos:
Acesso em linha: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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