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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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Dettagli Bibliografici
Pubblicato in:Blood
Autori principali: Mettananda, Sachith, Gibbons, Richard J., Higgs, Douglas R.
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Society of Hematology 2015
Soggetti:
Accesso online: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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