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Gene Addition Strategies for β-Thalassemia and Sickle Cell Anemia

Beta-thalassemia and sickle cell anemia are two of the most common diseases related to the hemoglobin protein. In these diseases, the beta-globin gene is mutated, causing severe anemia and ineffective erythropoiesis. Patients can additionally present with a number of life-threatening co-morbidities,...

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Publicado en:Adv Exp Med Biol
Autores principales: Dong, Alisa C., Rivella, Stefano
Formato: Artigo
Lenguaje:Inglês
Publicado: 2017
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5718882/
https://ncbi.nlm.nih.gov/pubmed/29127680
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-1-4939-7299-9_6
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