Fig. 2From: X-Linked retinoschisis associated to a novel intragenic microdeletion: case reportPartial electropherogram of exon 5 of RS1. Electropherogram of the proband showing a c.467_499 in-frame deletion mutation of 33 nucleotides leading to 11 amino acid deletion (RTDERLNWIYY – p.R156_Y166del)Back to article page