Fig. 1From: Psychomotor development and attention problems caused by a splicing variant of CNKSR2a Pedigree and Sanger sequencing confirmation of the splicing variant (c.1904 + 1G > A) of the CNKSR2 gene. b Schematic map of variant location and domains of the CNKSR2 gene. c Exon 16 skipping transcript detected from the patient caused by splicing variantBack to article page