A Novel Mutation Located in the N‐Terminal Domain of MYO15A Caused Sensorineural Hearing Loss

ABSTRACT Background MYO15A is one of the common genes of severe‐to‐profound sensorineural deafness. Mutations in this gene can cause both pre‐ and post‐lingual hearing losses. In this study, a novel MYO15A variant (c.2482C>T) was identified to be associated with autosomal recessive non‐syndromic...

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Published in:	Molecular Genetics & Genomic Medicine
Main Authors:	Yanli Wang, Zengping Liu, Yong Li, Zhipeng Nie, Baicheng Xu, Yiming Zhu, Shihong Duan, Xingjian Chen, Huan Tan, Jiong Dang, Minxin Guan, Yufen Guo
Format:	Article
Language:	English
Published:	Wiley 2024-12-01
Subjects:	deafness hair cell‐like cell induced pluripotent stem cells (iPSCs) MYO15A novel mutation
Online Access:	https://doi.org/10.1002/mgg3.70042