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Autor:
Essam Kerwash, Marija Sajic, Khadija Rerhou Rantell, James W. McBlane, John D. Johnston, Alison Niewiarowska, Andrew S. Butler, Susan Cole
Publikováno v:
Current Issues in Molecular Biology, Vol 46, Iss 8, Pp 8209-8225 (2024)
Sickle cell disease (SCD) and transfusion-dependent β-thalassemia (TDT) are hereditary haemoglobinopathies characterized by a reduction in functional β-globin chains. Both conditions cause tiredness and increase susceptibility to infection, which c
Externí odkaz:
https://doaj.org/article/b7972641d1d14bfaaa73db427cc7211b
