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Article

Distribution and frequencies of CDH23 mutations in Japanese patients with non-syndromic hearing loss.

Clinical genetics - 1 Oct 2007

Wagatsuma M, Kitoh R, Suzuki H, Fukuoka H, Takumi Y, Usami S

Abstract excerpt

Mutations in the CDH23 gene are known to be responsible for both Usher syndrome type ID (USH1D) and non-syndromic hearing loss (DFNB12), and the molecular confirmation of the CDH23 gene has become important in the diagnosis of these conditions. The present study was performed to find whether the...

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Source

Identifiers

PMID: 17850630
DOI: 10.1111/j.1399-0004.2007.00833.x

Genes

CDH23

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17850630-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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