Fig. 4From: Novel PPP1R21 mutation in a family with autosomal recessive neurodevelopmental disorder: results of genomics and molecular analysisA schematic section of the PPP1R21 gene, and the location of the identified pathogenic variant (c.1317_1318delAG) in human genome (GRCh38/hg38 assembly). Conservation of the region containing the mutation across different species is shown as wellBack to article page