Fig. 3From: Identification of a novel GLA mutation (Y88C) in a Korean family with Fabry nephropathy: a case reportElectropherogram of exon 2 of α-galactosidase A in this family with Fabry nephropathy. The analysis shows a mutation of A > G at nucleotide 263, resulting in an amino acid substitution p.Tyr88CysBack to article page