Cartas al EditorSíndrome hereditario de hiperferritinemia y cataratas: mutación de novo
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Cited by (4)
Ferritin L-subunit gene mutation and hereditary hyperferritinaemia cataract syndrome (HHCS): a case report and literature review
2021, Hematology (United Kingdom)Novel mutations in the ferritin-L iron-responsive element that only mildly impair IRP binding cause hereditary hyperferritinaemia cataract syndrome
2013, Orphanet Journal of Rare Diseases
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