Abstract
In this issue of Blood, Dubert et al present the results of a large cohort study conducted across 3 sub-Saharan African countries (Mali, Cameroon, and Ivory Coast) to quantify differences between subphenotypes of sickle cell disease (SCD) based on markers of anemia, hemolysis, and vascular complications.1
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CITATION STYLE
APA
Piel, F. B., & Williams, T. N. (2017, November 16). Subphenotypes of sickle cell disease in Africa. Blood. American Society of Hematology. https://doi.org/10.1182/blood-2017-10-808550
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