Skip to main content
Fig. 3 | BMC Infectious Diseases

Fig. 3

From: Correction to: Association of CMV genomic mutations with symptomatic infection and hearing loss in congenital CMV infection

Fig. 3

CMV variants in symptomatic and asymptomatic children. a Variant density of CMV genomes isolated from newborns (17 asymptomatic, 13 symptomatic) calculated in 1000 bp windows with Merlin as the reference strain. b Variants more frequent in symptomatic infection (Fisher’s exact test p < 0.05) are plotted with the genome position. The coding regions with the highest number of such variants are listed in their relative genomic position. c UL55 NSVs in relation to known antigenic domains (AD). Top panel shows the amino acid sequence of CMV strain Merlin. Bottom panel shows where NSVs (indicated by arrows below the reference strain) are more likely seen in infants with symptomatic congenital CMV in relation to antigenic domains

Back to article page