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Article

Cellular origin of fundus autofluorescence in patients and mice with a defective NR2E3 gene.

The British journal of ophthalmology - 1 Sept 2009

Wang N-K, Fine H F, Chang S, Chou C L, Cella W, Tosi J, Lin C-S, Nagasaki T, Tsang S H

Abstract excerpt

AIM: To characterise new clinical features in a family with enhanced S-cone syndrome (ESCS) and investigate the pathogenesis of these clinical features in the homozygous Nr2e3(rd7) (rd7) mutant mice. METHODS: Four patients from an affected family were included for genotypic and phenotypic study. Eye tissues from rd7 mice were used to detect a possible relationship between macrophages and autofluorescent material...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 19429590
DOI: 10.1136/bjo.2008.153577
PMCID: PMC2742679

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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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