M Cicilano, G Zecchina, A Roetto, S Bosio, V Infelise, S Stefani, U Mazza, C Camaschella. Recurrent mutations in the iron regulatory element of L-ferritin in hereditary hyperferritinemia-cataract syndrome. haematol [Internet]. 1999Jun.1 [cited 2024May3];84(6):489-92. Available from: https://haematologica.org/article/view/1386