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Article

Simultaneous MT-RNR1 and MYO15A Mutations in a Family with Non-Syndromic Hearing Loss.

The journal of international advanced otology - 29 Sept 2025

Chen Yiyuan, Yang Run, Chen Ying, Zhang Tianyu, Ma Jing

Abstract excerpt

UNLABELLED: Congenital hearing loss is one of the prevalent birth defects, with approximately 60% of cases attributed to genetic factors. Genetic hearing loss is broadly classified into syndromic and non-syndromic forms, with non-syndromic hearing loss accounting for 70% of cases. MYO15A mutations are known to cause autosomal recessive non-syndromic hearing loss (ARNSHL), while MT-RNR1 mutations follow a maternal...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 42378530
DOI: 10.5152/iao.2025.241817
PMCID: PMC12520145

Genes

MYO15A

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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