Fig. 2From: An overview of the multi-pronged approach in the diagnosis of Alport syndrome for 22 children in Northeast Chinaa The family pedigree of P2. The proband’s mother has persistent hematuria and proteinuria with unknown cause and his grandfather died of uremia. b Genomic analysis. WES results of the patient and his parents indicate that P2 has one variant in the COL4A5 gene: c.[2890G>T], p.(G964X), exon33, chrX:107866028, inherited from his motherBack to article page