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Transferrin receptor 2 (Tfr2) genetic deletion makes transfusion‐independent a murine model of transfusion‐dependent β‐thalassemia
β‐thalassemia is a genetic disorder caused by mutations in the β‐globin gene, and characterized by anemia, ineffective erythropoiesis and iron overload. Patients affected by the most severe transfusion‐dependent form of the disease (TDT) require lifelong blood transfusions and iron chelation therapy...
Autores principales: | Di Modica, Simona Maria, Tanzi, Emanuele, Olivari, Violante, Lidonnici, Maria Rosa, Pettinato, Mariateresa, Pagani, Alessia, Tiboni, Francesca, Furiosi, Valeria, Silvestri, Laura, Ferrari, Giuliana, Rivella, Stefano, Nai, Antonella |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540808/ https://www.ncbi.nlm.nih.gov/pubmed/36071579 http://dx.doi.org/10.1002/ajh.26673 |
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