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TMPRSS6/matriptase‐2 is essential for maintaining proper systemic iron balance through its negative regulation of hepatic hepcidin production. Loss-of-function mutations result in severe hereditary anemia due to unrestrained suppression of intestinal and tissue-derived plasma iron supply.
siRNA-mediated silencing of Tmprss6 led to increased hepatic hepcidin mRNA and reduced transferrin saturation
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