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The prototypic genetic deficiency is loss-of-function mutations in the gene encoding the protein proFLG (Hoober and Eggink, 2022

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Global heterogeneity in folic acid fortification policies and implications for prevention of neural tube defects and stroke: a systematic review

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The solution can be administered intramuscularly or subcutaneously, depending on the severity of the patient's condition

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Red blood cells are responsible for carrying oxygen through the body

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