Article

Association of a novel missense mutation in MYO15A with nonsyndromic hearing loss: a case report

2020-06-17

Abstract excerpt

<h4>Background: </h4> Hearing loss is a common disease globally, and more than 50% of the cases are genetic. Autosomal recessive nonsyndromic hearing loss (ARNSHL) is one of the most common types of hereditary hearing loss. Here, a novel MYO15A missense mutation was identified in a Chinese family with ARNSHL, using targeted genetic sequencing and Sanger sequencing. Case presentation: A 6-year-old girl with congen...

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Literature Corpus work: 4e08cc0d-a42e-5126-a819-1fe586d69496
DOI: 10.21203/rs.3.rs-34119/v1

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