Article

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

2019-12-27

Abstract excerpt

<title>Abstract</title> <p>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. <h4>Methods:</h4> In the current study , we reported a polygenic mode of inheritance in an NSHL consangui...

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Literature Corpus work: 9c4e6217-5e10-59d4-8365-19b032483f0a
DOI: 10.21203/rs.2.13328/v6

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