Similar content being viewed by others Introduction Sickle cell disease (SCD) is an inherited hematological disorder caused by an A to T mutation in the adult -globin gene with the product of hemoglobin S which polymerizes under hypoxia conditions 1,2
Fourth, we identified one intronic variant on chromosome 16 in the MAFTRR and LOC105371356 genes, both of which affect thyroid function, indicating a potential link between thyroid-related pathways and POAG susceptibility 69
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