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Curing Hemoglobinopathies: Challenges and Advances of Conventional and New Gene Therapy Approaches
Inherited hemoglobin disorders, including beta-thalassemia (BT) and sickle-cell disease (SCD), are the most common monogenic diseases worldwide, with a global carrier frequency of over 5%.1 With migration, they are becoming more common worldwide, making their management and care an increasing concer...
Tallennettuna:
| Julkaisussa: | Mediterr J Hematol Infect Dis |
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| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Università Cattolica del Sacro Cuore
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6827604/ https://ncbi.nlm.nih.gov/pubmed/31700592 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4084/MJHID.2019.067 |
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