Giansily-Blaizot, M., Cunat, S., Moulis, G., Schved, J., & Aguilar-Martinez, P. (2013). Homozygous mutation of the 5'UTR region of the L-Ferritin gene in the hereditary hyperferritinemia cataract syndrome and its impact on the phenotype. Ferrata Storti Foundation.
শিকাগো স্টাইলে সাইটেশনGiansily-Blaizot, Muriel, Séverine Cunat, Grégory Moulis, Jean-François Schved, এবং 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. Ferrata Storti Foundation, 2013.
এমএলএ সাইটেশনGiansily-Blaizot, Muriel, et al. Homozygous Mutation of the 5'UTR Region of the L-Ferritin Gene in the Hereditary Hyperferritinemia Cataract Syndrome and Its Impact On the Phenotype. Ferrata Storti Foundation, 2013.