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Article

Cdh23 mutations in the mouse are associated with retinal dysfunction but not retinal degeneration.

Experimental eye research - 1 Dec 2003

Libby Richard T, Kitamoto Junko, Holme Ralph H, Williams David S, Steel Karen P

Abstract excerpt

Mutations in the cadherin 23 gene (CDH23) cause Usher syndrome type 1D in humans, a disease that results in retinitis pigmentosa and deafness. Cdh23 is also mutated in the waltzer mouse. In order to determine if the retina of the waltzer mouse undergoes retinal degeneration and to gain insight into the function of cadherin 23 in the retina, we have characterized the anatomy and physiology of retinas of waltzer...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 14609561
DOI: 10.1016/j.exer.2003.07.007

Genes

ERG
CDH23

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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Cdh23 mutations in the mouse are associated with retinal dysfunction but not retinal degeneration.PMID 14609561Read ↗

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