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Article

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity - 1 Jan 2026

Zhu Yajing, Wang Tianyu, Sun Xianglan, Lin Bojian, Liu Huanhai, Chen Li, Cheng Yin, Peng Hu

Abstract excerpt

BACKGROUND: Hearing loss is the most common sensory nervous system defect in humans. Approximately half of hearing loss cases have a genetic etiology. At present, more than 300 genes and 1000 mutations have been identified that cause hereditary hearing loss (HHL). However, there are still a large number of unknown genes related to hearing loss. OBJECTIVE: The purpose of this study was to analyze the clinical...

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Identifiers

PMID: 42657483
DOI: 10.1155/np/4050645
PMCID: PMC13519884

Genes

ACTG1

Variants

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