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Article

The Enigma of CRB1 and CRB1 Retinopathies.

Advances in experimental medicine and biology - 1 Jan 2019

Ray Thomas A, Cochran Kelly J, Kay Jeremy N

Abstract excerpt

Mutations in the gene Crumbs homolog 1 (CRB1) are responsible for several retinopathies that are diverse in severity and phenotype. Thus, there is considerable incentive to determine how disruption of this gene causes disease. Progress on this front will aid in developing molecular diagnostics that can predict disease severity with the ultimate goal of developing therapies for CRB1 retinopathies via gene...

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PMID: 31884620
DOI: 10.1007/978-3-030-27378-1_41

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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