Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF

Hearing loss (HL) represents the most common congenital sensory impairment with an incidence of 1 –5 per 1000 live births. Non-syndromic hearing loss (NSHL) is an isolated finding that is not part of any other ...

Source: BMC Medical Genetics - January 2, 2020 Category: Genetics & Stem Cells Authors: Athar Khalil, Samer Bou Karroum, Rana Barake, Gabriel Dunya, Samer Abou-Rizk, Amina Kamar, Georges Nemer and Marc Bassim Tags: Research article Source Type: research