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β-thalassemia major is an inherited hemoglobinopathy that requires lifelong red blood cell transfusions and iron chelation therapy to prevent complications due to iron overload. Traditionally, β-thalassemia has been more common in certain regions o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::05a7095188caa8a4acd1013d80dbb3b5
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3103520
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3103520