Fig. 3From: Two novel mutations in the ALPL gene of unrelated Chinese children with Hypophosphatasia: case reports and literature reviewSchematic drawing of the ALPL gene mutations identified in Chinese HPP patients. The position of all identified mutations are indicated. The mutations reported previously are indicated in black, while six mutations identified in the present study are indicated in red and blue. The red color highlights the novel mutations, and the blue color represents the pathogenic mutations reported previously, whereas italic font with underline represents the mutations detected in two patientsBack to article page