Fig. 4From: Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentationSummary of KITLG gene mutations associated with FPHH. All the mutations associated with FPHH are located within the VTNNV region in exon 2, except c.337G > A in exon 4 of the KITLG gene. The mutations reported previously are in BLUE, while the novel mutation (c.104A > T) at 35 N reported in this study is in REDBack to article page