For example, mutations in RpS19, RpS17, RpS24, RpL35a, RpS7, RpL5, RpL11, RpS10 and RpS26 have been associated with the human disease Diamond Blackfan Anemia (DBA), a dominant autosomal bone marrow failure syndrome, characterised by hypoplastic anemia with a predisposition to leukemia [13]–[19]. The gene discussed is RPS26; the disease is Diamond-Blackfan anemia.