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Publikováno v:
Physiology. 38
Background: Sickle cell disease (SCD) is an autosomal recessive blood disorder caused by mutations in the β-globin gene, resulting in hemoglobin S (HbS) polymerization and red blood sickling. SCD patients carry two copies of the mutant HbS (HbSS) an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47eafc70fd7ef5f9fa8c347aad1e9bc4
https://doi.org/10.1152/physiol.2023.38.s1.5731525
https://doi.org/10.1152/physiol.2023.38.s1.5731525
