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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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Dades bibliogràfiques
Publicat a:Blood
Autors principals: Mettananda, Sachith, Gibbons, Richard J., Higgs, Douglas R.
Format: Artigo
Idioma:Inglês
Publicat: American Society of Hematology 2015
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Accés en línia: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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