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Autor:
LFS Gushiken, SL Linguet, EMF Gotardo, PL Brito, FC Leonardo, CLV Kim, S Laurance, B Koehl, FF Costa, N Conran
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S99-S100 (2024)
Introduction: Sickle cell disease (SCD), the most common inherited hemoglobinopathy worldwide, results in the production of abnormal hemoglobin S. Polymerization of this hemoglobin causes red blood cell sickling and pathophysiological consequences. V
Externí odkaz:
https://doaj.org/article/62e5740a40504b8f93dac87b926fde3a
