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Gene Therapy in Thalassemia and Hemoglobinopathies
Sickle cell disease (SCD) and ß-thalassemia represent the most common hemoglobinopathies caused, respectively, by the alteration of structural features or deficient production of the ß-chain of the Hb molecule. Other hemoglobinopathies are characterized by different mutations in the α- or ß-globin g...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Università Cattolica del Sacro Cuore
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3033156/ https://ncbi.nlm.nih.gov/pubmed/21415990 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4084/MJHID.2009.008 |
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