[1]
Kamilia, B., Mouloud, Y., Moez, G., Fadhila, B., Ilhem, B.C. and Wiem, M. 2017. The predominance of codon 39 (c>t) mutation of HBB gene in a portion of the Algerian population (Northeast Algeria). Journal of Biological Research - Bollettino della Società Italiana di Biologia Sperimentale. 90, 1 (Apr. 2017). DOI:https://doi.org/10.4081/jbr.2017.6407.