The audiological phenotype of patients with a variant in MYH9 and MYH14 genes

Abstract Mutations in MYH9 and MYH14 are associated with autosomal dominant, progressive sensorineural hearing loss. This study aimed to characterize and compare the clinical and audiological features of patients with MYH9 or MYH14 variants. Thirteen patients with MYH9 or MYH14 mutations were identi...

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Bibliographic Details
Main Authors: Seong Hoon Bae, Sun Young Joo, Seung Hyeon Jang, Sung Huhn Kim, Jae Young Choi, Dongju Won, Heon Yung Gee, Jinsei Jung
Format: Article
Language:English
Published: Nature Portfolio 2025-07-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-025-08801-w
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