Thalassemia is caused by a mutation that reduces or prevents the synthesis of one of the globin chains (α or β), resulting in a quantitative defect. Sickle Cell Anaemia, on the other hand, is due to a point mutation in the β-globin gene, which causes the production of abnormal hemoglobin S—this is a qualitative defect. Thus, the correct statement is that thalassemia is due to reduced (less) synthesis of globin molecules.