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

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

Abstract Background 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 disorder accounting for 70% of all genetic hearing loss cases. Methods...

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Main Authors: Athar Khalil (Author), Samer Bou Karroum (Author), Rana Barake (Author), Gabriel Dunya (Author), Samer Abou-Rizk (Author), Amina Kamar (Author), Georges Nemer (Author), Marc Bassim (Author)
Format: Book
Published: BMC, 2020-01-01T00:00:00Z.
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3rd Floor Main Library

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