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January 1, 2019Otorhinolaryngology-Head and Neck SurgeryOpen Access

A novel compound heterozygous mutation in the MYO15A gene in autosomal recessive hearing loss identified by targeted massively parallel sequencing

Guang‐Jie Zhu Dengbin Ma Lusen Shi Han Zhou Jie Chen Xia Gao

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Abstract

Objectives: Inherited genetic defects are the most common causes of autosomal recessive nonsyndromic hearing loss (ARNSHL), affecting millions of people worldwide. Identification and specific molecular diagnosis of the pathogenic genes or loci would facilitate basic research of ARNSHL and its clinical prevention and treatment.

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Zhu et al. (2019) studied this question.

synapsesocial.com/papers/6a9fb9d71cf0e01ec7bab514 https://doi.org/10.15761/ohns.1000207

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