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Secondary folic acid deficiency The molecular basis of the inherited folate absorption disorder is a mutation in the SLC46A1 gene, which encodes the proton-coupled folate transporter (PCFT)

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Anatomy & Pathophysiology Erythropoiesis and Red Blood Cell Physiology Red blood cells (erythrocytes) are produced in the bone marrow via erythropoiesis, a process regulated primarily by erythropoietin (EPO) , a glycoprotein hormone produced by peritubular cells of the renal cortex in response to tissue hypoxia

It helps counteract some of the fatigue or sluggishness that can occur during periods of appetite suppression or rapid weight loss