Marked microcytosis and increased transferrin saturation: Think about variants in SLC11A2 (DMT1)
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Congenital microcytic anemias are rare diseases associated with decreased hemoglobin synthesis and red blood cells of low corpuscular volume. DMT1/NRAMP2 is a highly conserved divalent cation transporter encoded by the SLC11A2 gene, expressed at the membrane o... ...
