Fig. 5From: Novel PPP1R21 mutation in a family with autosomal recessive neurodevelopmental disorder: results of genomics and molecular analysisSequencing chromatogram of genomic DNA showing c.1317_1318delAG; p.(Asp440Tyrfs*6) mutation in PPP1R21 gene. The patient was homozygous for this variant, and the parents were heterozygousBack to article page