Ferritin light chain gene mutations in two Brazilian families with hereditary hyperferritinemia-cataract syndrome

por Petroni, Roberta Cardoso, da Rosa, Susana Elaine Alves, de Carvalho, Flavia Pereira, Santana, Rúbia Anita Ferraz, Hyppolito, Joyce Esteves, Nascimento, Claudia Mac Donald Bley, Hamerschlak, Nelson, Campregher, Paulo Vidal
Publicado 2017