Fig. 4From: Identification of a novel WAS mutation and the non-splicing effect of a second-site mutation in a Chinese pedigree with Wiskott–Aldrich syndromea Mutation analysis of WAS gene in the proband (hemizygous mutation of c.158 T > C in exon 2, p.L53P); b Sequencing analysis of WAS gene in the proband’s mother (heterozygous mutation of c.158 T > C); c Sequencing analysis of WAS gene in the proband’s father (wild-type with no mutation)Back to article page