Article

Identification of a novel mutation of EYA4 in a Chinese family with delayed nonsyndromic hearing loss and analysis of molecular epidemiology of EYA4 mutations

2024-03-25

Abstract excerpt

<title>Abstract</title> <p><bold>Background</bold>: <italic>EYA4</italic> is responsible for <italic>DFNA10</italic> deafness. Because of its insidious onset and slow progression, hearing loss in ADSHL is usually difficult to detect early in clinical settings and the intervention is relatively backward. Genetic testing can help to detect hearing loss early and facilitate early intervention, effectively reducing t...

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Literature Corpus work: c7d3ec4d-d4d9-5be7-8088-6383c9b3bbc5
DOI: 10.21203/rs.3.rs-4115584/v1

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