Case Report
Coinheritance of the c.-19 G > C and c.315 + 1 G > A Variants in the β-Globin Gene Leads to Thalassemia Disease: A Report from the North of Iran
Figure 2
The results of capillary electrophoresis on the mother’s blood showed a normal pattern, despite having c.-19 G > C variant. The mother has a normal HbA2 level, even though she carries the c.-19 G > C mutation.