Fig. 1From: Identification of compound heterozygous patients with primary hyperoxaluria type 1: clinical evaluations and in silico investigations a Pedigree of the Family F1 showing the inheritance of the c.32C > T, c.731 T > C and c.33_34insC mutations in the affected members P1, P2 and P3. b Pedigree of the Family F2 showing the inheritance of the c.26C > A and c.65A > G variations in the affected members P4Back to article page