Novel mutations in the ferritin-L iron-responsive element that only mildly impair IRP binding cause hereditary hyperferritinaemia cataract syndrome - Luscieti, Sara; Tolle, Gabriele; Aranda, Jessica; Campos, Carmen Benet; Risse, Frank; Morán, Érica; Muckenthaler, Martina; Sánchez, Mayka (Orphanet journal of rare diseases, 2013)
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