Petroni, R. C., da Rosa, S. E. A., de Carvalho, F. P., Santana, R. A. F., Hyppolito, J. E., Nascimento, C. M. D. B., . . . Campregher, P. V. (2017). Ferritin light chain gene mutations in two Brazilian families with hereditary hyperferritinemia-cataract syndrome. Einstein (Sao Paulo).

Petroni, Roberta Cardoso, Susana Elaine Alves da Rosa, Flavia Pereira de Carvalho, Rúbia Anita Ferraz Santana, Joyce Esteves Hyppolito, Claudia Mac Donald Bley Nascimento, Nelson Hamerschlak, và Paulo Vidal Campregher. "Ferritin Light Chain Gene Mutations in Two Brazilian Families With Hereditary Hyperferritinemia-cataract Syndrome." Einstein (Sao Paulo) 2017.

Petroni, Roberta Cardoso, et al. "Ferritin Light Chain Gene Mutations in Two Brazilian Families With Hereditary Hyperferritinemia-cataract Syndrome." Einstein (Sao Paulo) 2017.