Clinical and genetic factors are associated with pain and hospitalisation rates in sickle cell anaemia in Cameroon.
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Wonkam Ambroise, Mnika Khuthala, Ngo Bitoungui Valentina J, Chetcha Chemegni Bernard, Chimusa Emile R, Dandara Collet, Kengne Andre
DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.
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Lettre Guillaume, Sankaran Vijay G, Bezerra Marcos André C, Araújo Aderson S, Uda Manuela, Sanna Serena, Cao Antonio, Schlessinger David, Costa Fernando F, Hirschhorn Joel N, Orkin Stuart