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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Detalles Bibliográficos
Autores principales: Finotti, Alessia, Breda, Laura, Lederer, Carsten W, Bianchi, Nicoletta, Zuccato, Cristina, Kleanthous, Marina, Rivella, Stefano, Gambari, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4342371/
https://www.ncbi.nlm.nih.gov/pubmed/25737641
http://dx.doi.org/10.2147/JBM.S46256

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4342371/
https://www.ncbi.nlm.nih.gov/pubmed/25737641
http://dx.doi.org/10.2147/JBM.S46256

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