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Article

Cone structure in patients with usher syndrome type III and mutations in the Clarin 1 gene.

JAMA ophthalmology - 1 Jan 2013

Ratnam Kavitha, Västinsalo Hanna, Roorda Austin, Sankila Eeva-Marja K, Duncan Jacque L

Abstract excerpt

OBJECTIVE: To study macular structure and function in patients with Usher syndrome type III (USH3) caused by mutations in the Clarin 1 gene (CLRN1). METHODS: High-resolution macular images were obtained by adaptive optics scanning laser ophthalmoscopy and spectral domain optical coherence tomogra...

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Source

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Identifiers

PMID: 22964989
DOI: 10.1001/2013.jamaophthalmol.2
PMCID: PMC4482614

Genes

CLRN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22964989-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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