Autosomal recessive non-syndromic hearing loss is one of the most common monogenic diseases. It is characterized by high allelic and locus heterogeneities that make a precise diagnosis difficult. In this study. whole-exome sequencing was performed for an affected patient allowing us to identify a new frameshift mutation (c. https://ashleyshomestores.shop/product-category/outdoor-armless-chair-with-cushion/