Belhadi , K., GribaaMoez, H. Djaara, and OuarhlentYamina. “The First Association of Hb Knossos: (HBB: c.82G>T) With (HBB: C.118C˃T) Mutation Causes Thalassemia Homozygous in Algerian Children”. GSC Biological and Pharmaceutical Sciences, vol. 12, no. 1, July 2020, pp. 162-97, doi:10.30574/gscbps.2020.12.1.0192.