Fig. 1
From: De novo POGZ mutations in sporadic autism disrupt the DNA-binding activity of POGZ
Schematic structure of POGZ and its putative functional domains. The ASD-(upper) and ID- (lower) associated de novo mutations are indicated below the protein. Bold mutations, common de novo mutations between ASD and ID. Note that the R1001X mutation was found in ID and ASD/ID patients. X, nonsense; del, deletion; fs, frameshift; *, premature stop codon