Fig. 4From: Correction to: Association of CMV genomic mutations with symptomatic infection and hearing loss in congenital CMV infectionCMV variation from children with normal hearing and SNHL. Variant density of CMV genomes isolated from 17 children with normal hearing and 13 children with SNHL calculated in a 1000 bp sliding window with Merlin as the reference strain. Variants more frequent in viruses from children with SNHL (Fisher’s exact test p < 0.05) are plotted with the genome position. The coding regions with the highest number of variants are listed with the genomic positionBack to article page