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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Detalles Bibliográficos
Autores principales: Breda, Laura, Gambari, Roberto, Rivella, Stefano
Formato: Texto
Lenguaje:English
Publicado: Università Cattolica del Sacro Cuore 2009
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033156/
https://www.ncbi.nlm.nih.gov/pubmed/21415990
http://dx.doi.org/10.4084/MJHID.2009.008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033156/
https://www.ncbi.nlm.nih.gov/pubmed/21415990
http://dx.doi.org/10.4084/MJHID.2009.008

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