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Article

The natural history of OPA1-related autosomal dominant optic atrophy.

The British journal of ophthalmology - 1 Oct 2008

Cohn A C, Toomes C, Hewitt A W, Kearns L S, Inglehearn C F, Craig J E, Mackey D A

Abstract excerpt

BACKGROUND/AIMS: Autosomal dominant optic atrophy (ADOA) is a genetically heterogenous disease. However, a large proportion of this disease is accounted for by mutations in OPA1. The aim of this longitudinal study was to investigate disease progression in Australian ADOA patients with confirmed O...

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Source

Identifiers

PMID: 18653586
DOI: 10.1136/bjo.2007.134726

Genes

OPA1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18653586-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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