Biological impact of α genes, β haplotypes, and G6PD activity in sickle cell anemia at baseline and with hydroxyurea - Bernaudin, Françoise; Arnaud, Cécile; Kamdem, Annie; Hau, Isabelle; Lelong, Françoise; Epaud, Ralph; Pondarré, Corinne; Pissard, Serge (Blood advances, 2018)
Keywords: alpha-Globins - genetics; Anemia, Sickle Cell - diagnosis; Anemia, Sickle Cell - drug therapy; Anemia, Sickle Cell - genetics; Anemia, Sickle Cell - metabolism; beta-Globins - genetics; Biomarkers; Enzyme Activation; Female; Fetal Hemoglobin - genetics; Genetic Association Studies; Genetic Predisposition to Disease; Global Advances; Glucosephosphate Dehydrogenase - metabolism; Glucosephosphate Dehydrogenase Deficiency - genetics; Glucosephosphate Dehydrogenase Deficiency - metabolism; Haplotypes; Humans; Hydroxyurea - therapeutic use; Male; Polymorphism, Single Nucleotide; Prevalence; Promoter Regions, Genetic; Red Cells, Iron, and Erythropoiesis; Risk Factors; Treatment Outcome