Figure 1From: Multiphasic analysis of whole exome sequencing data identifies a novel mutation of ACTG1 in a nonsyndromic hearing loss familyNSHL family pedigree and clinical features. Pedigree with phenotype and experimental information. Black and white denote affected and unaffected subjects, respectively, while shaded grey represents equivocal hearing status (A). Typical audiograms of affected and unaffected subjects (B). Scheme of the multiphasic analysis of WES data (C).Back to article page