Molecular basis for the recently described hereditary hyperferritinemia-cataract syndrome: a mutation in the iron-responsive element of ferritin L-subunit gene (the "Verona mutation")

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Published in Blood on December 01, 1995

Authors

D Girelli1, R Corrocher, L Bisceglia, O Olivieri, L De Franceschi, L Zelante, P Gasparini

Author Affiliations

1: Institute of Medical Pathology, University of Verona, Italy.

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