Muriel Giansily-Blaizot, Séverine Cunat, Grégory Moulis, Jean-François Schved, Patricia Aguilar-Martinez. Homozygous mutation of the 5’UTR region of the L-Ferritin gene in the hereditary hyperferritinemia cataract syndrome and its impact on the phenotype. haematol [Internet]. 2013Mar.31 [cited 2024Nov.25];98(4):e42-e43. Available from: https://haematologica.org/article/view/6640