Figure 3
From: A novel DSPPmutation causes dentinogenesis imperfecta type II in a large Mongolian family
Identification of a novel mutation. An A→G transition adjacent to the donor splicing site (GT) within intron 3 of DSPP was detected in all affected individuals, whereas this mutation was not detected in unaffected individuals of the DGI-II Mongolian family or in unrelated healthy Mongolian controls. DNA sequences for a normal family member (upper panel) and the proband IV5 (lower panel).