Fig. 2From: The biallelic novel pathogenic variants in AGL gene in a chinese patient with glycogen storage disease type IIIPedigree of the GSD III family with the variants of exon 5 and exon 13. Here, the circles indicate female individuals and rectangles indicate males. The patient of the study is indicated by a black circle. The patient (II-2) contains two variations in AGL gene, the c.597delG(p.Q199Hfs※2)in exon 5 is inherited from the mother (I-2) and the deletion of exon 13 is inherited from the father(I-1)Back to article page