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Changing patterns in the epidemiology of β‐thalassemia

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 of the world such as the Mediterranean, Middle East,...

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Dades bibliogràfiques
Publicat a:Eur J Haematol
Autors principals: Kattamis, Antonis, Forni, Gian Luca, Aydinok, Yesim, Viprakasit, Vip
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2020
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7692954/
https://ncbi.nlm.nih.gov/pubmed/32886826
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ejh.13512
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