Aceruloplasminemia is caused by biallelic mutations in the CP gene, a 20 exons gene encompassing approximately 65 kb of DNA, located in chromosome locus 3q24-q25 and encoding CP (Yoshida et al., 1995; Hellman and Gitlin, 2002; Kono, 2013). This evidence concerns the gene CP and aceruloplasminemia.