Fig. 2From: Stargardt disease-associated in-frame ABCA4 exon 17 skipping results in significant ABCA4 functionVariant c.2653+1G>A results in complete skipping of exon 17. The ABCA4 genomic sequence flanked by rhodopsin exons 3 and 5. cDNA products were amplified using primers situated in exons 16 and 18, represented with triangles. The mutant construct shows complete exon 17 skipping as shown by Sanger sequencingBack to article page