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Article

Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populations.

Investigative ophthalmology & visual science - 1 Mar 2013

Beryozkin Avigail, Zelinger Lina, Bandah-Rozenfeld Dikla, Harel Anat, Strom Tim A, Merin Saul, Chowers Itay, Banin Eyal, Sharon Dror

Abstract excerpt

PURPOSE: We evaluated the role of Crumbs homolog 1 (CRB1) in autosomal recessive (AR) retinal diseases in the Israeli and Palestinian populations using homozygosity mapping. METHODS: Clinical analysis included family history, ocular examination, full-field electroretinography (ERG), and funduscop...

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Source

Identifiers

PMID: 23449718
DOI: 10.1167/iovs.12-11419

Genes

CRB1
ERG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23449718-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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