BELHADI , K.; GRIBAAMOEZ; DJAARA , H.; 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, [S. l.], v. 12, n. 1, p. 162–197, 2020. DOI: 10.30574/gscbps.2020.12.1.0192. Disponível em: https://gsconlinepress.com/journals/index.php/gscbps/article/view/gscbps-2020-0192. Acesso em: 25 nov. 2024.