1-1 of 1
Luigi Bisceglia
Close
Sort by
Journal Articles

Hereditary Hyperferritinemia-Cataract Syndrome Caused by a 29-Base Pair Deletion in the Iron Responsive Element of Ferritin L-Subunit Gene

Domenico Girelli, Roberto Corrocher, Luigi Bisceglia, Oliviero Olivieri, Leopoldo Zelante, Giacomo Panozzo, Paolo Gasparini
Journal: Blood
Blood (1997) 90 (5): 2084–2088.
https://doi.org/10.1182/blood.V90.5.2084
Published: 1997