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Article

Genetic analysis of CLDN14 in the Chinese population affected with non-syndromic hearing loss.

International journal of pediatric otorhinolaryngology - 1 Feb 2018

Lu Yajie, Yao Jun, Wei Qinjun, Xu Jin, Xing Guangqian, Cao Xin

Abstract excerpt

OBJECTIVE: The CLDN14 gene, encoding the tight junction protein Claudin-14, has been proposed as a candidate causative gene affecting autosomal recessive non-syndromic hearing loss (ARNSHL). Genetic analysis of nonsynonymous single-nucleotide variations (nsSNVs) in CLDN14 has been performed in different populations. The role of CLDN14 nsSNVs in contributing to hearing loss in Chinese populations would be...

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Source

Identifiers

PMID: 29447821
DOI: 10.1016/j.ijporl.2017.11.016

Genes

CLDN14

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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