Novel mutation in the ASXL3 gene in a Chinese boy with microcephaly and speech impairment: A case report

Figure 3 ASXL3 mutations identified in patients with Bainbridge-Ropers syndrome to date (including the novel variant of this study). Novel variant is indicated by underline and italics. The recurrent mutations are indicated in bold. The mutations located in the ASXH domain are in blue rectangular boxes. The mutations located in the ASXM1 domain are in orange rectangular boxes. The mutation located in plant homeodomain finger is in a red rectangular box. PHD: Plant homeodomain.