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Recent trends in the gene therapy of β-thalassemia
The β-thalassemias are a group of hereditary hematological diseases caused by over 300 mutations of the adult β-globin gene. Together with sickle cell anemia, thalassemia syndromes are among the most impactful diseases in developing countries, in which the lack of genetic counseling and prenatal dia...
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| Publicat a: | J Blood Med |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Dove Medical Press
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4342371/ https://ncbi.nlm.nih.gov/pubmed/25737641 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/JBM.S46256 |
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