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Article

Reduction of inner retinal thickness in patients with autosomal dominant optic atrophy associated with OPA1 mutations.

Investigative ophthalmology & visual science - 1 Sept 2007

Ito Yasuki, Nakamura Makoto, Yamakoshi Tomomi, Lin Jian, Yatsuya Hiroshi, Terasaki Hiroko

Abstract excerpt

PURPOSE: To determine the morphologic changes in the retina in the macula and around the optic disc in patients with autosomal dominant optic atrophy (ADOA) associated with a mutation in the OPA1 gene. METHODS: Cross-sectional images of the macular area of the retina were obtained by optical coherence tomography (OCT) in patients with ADOA who had a heterozygous mutation in the OPA1 gene. There were 15 eyes of...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17724190
DOI: 10.1167/iovs.07-0024

Genes

OPA1

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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