Article

Identification of novel gene variants causing autosomal recessive non-syndromic hearing loss in Iranian families

2024-02-20

Abstract excerpt

<title>Abstract</title> <p>Background Hearing loss (HL) is known as the most common sensory disorder in humans, with an incidence in 466 million people worldwide. This disorder is genetically highly heterogeneous, so that among the 180 genes responsible for HL, a disproportionate share of genes is involved in different ethnicities. Here, we report the underlying genetic cause of non-syndromic hearing loss (NSHL)...

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Literature Corpus work: f0360126-7622-5f76-99f1-9c5000ad0bf1
DOI: 10.21203/rs.3.rs-3940905/v1

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