Article

Novel MYO15A Variants are Associated with Hearing Loss in the Two Iranian Pedigrees

2020-11-13

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> Clinical genetic diagnosis of non-syndromic hearing loss (NSHL) is quite challenging. With regard to its high heterogeneity as well as large size of some genes, it is also really difficult to detect causative mutations using traditional approaches. One of the recent technologies called whole-exome sequencing (WES) has been thus developed in this domain to remove...

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Literature Corpus work: c553424d-8059-50af-acf6-fb6be49103b8
DOI: 10.21203/rs.2.19322/v5

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