M-I Moreno-Carralero

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To the Editor : Hereditary hyperferritinemia cataract syndrome (HHCS) (MIM 600886) is caused by mutations in the iron responsive element (IRE) on the 5′ untranslated region of the L-ferritin gene (FTL). The IRE binds to cytoplasmic iron regulatory proteins forming a complex that controls the FTL mRNA translation depending on the iron status; mutations in(More)
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