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Article

Prevalence and clinical features of hearing loss patients with CDH23 mutations: a large cohort study.

PloS one - 1 Jan 2012

Miyagawa Maiko, Nishio Shin-ya, Usami Shin-ichi

Abstract excerpt

Screening for gene mutations in CDH23, which has many exons, has lagged even though it is likely to be an important cause for hearing loss patients. To assess the importance of CDH23 mutations in non-syndromic hearing loss, two-step screening was applied and clinical characteristics of the patien...

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Identifiers

PMID: 22899989
DOI: 10.1371/journal.pone.0040366
PMCID: PMC3416829

Genes

CDH23

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22899989-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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