These hypotheses on the genetic relatedness of Mauritanian white Moors and peoples dwelling in North Africa today could be further strengthened by performing genetic analysis of other codons that have been reported to undergo unique mutations in some Algerian and Moroccan subjects with G6PD deficiency, such as the Kabyle and Aures G6PD A- variants [22,23,29]. The gene discussed is G6PD; the disease is G6PD deficiency.