Implication of HMOX1 and CCR5 genotypes on clinical phenotype of Egyptian patients with sickle cell anemia
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DOI: 10.1007/s00277-019-03697-9
Abstract: Sickle cell disease (SCD) is a relatively common inherited hemolytic anemia among individuals of African descent. Genetic factors might clarify clinical diversity of the disease and variations in treatment response. Some researchers investigated heme oxygenase-1… read more here.
Keywords: ccr5 genotypes; disease; ccr5; sickle cell ... See more keywords