Fig. 3From: A novel homozygous splice site variant in ARL2BP causes a syndromic autosomal recessive rod-cone dystrophy with situs inversus, asthenozoospermia, unilateral renal agenesis and microcystsChromatic Full-field stimulus threshold testing. Legend Chromatic FST show similar responses between cone and rod mediated thresholds in both eyes suggesting functional loss of rod vision and cone-mediation for all stimuliBack to article page