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Article

The natural history of stargardt disease with specific sequence mutation in the ABCA4 gene.

Investigative ophthalmology & visual science - 1 Dec 2009

Genead Mohamed A, Fishman Gerald A, Stone Edwin M, Allikmets Rando

Abstract excerpt

PURPOSE: To determine longitudinal changes in fundus appearance and visual function in patients with Stargardt with at least one allelic mutation (Gly1961Glu) in the ABCA4 gene. METHODS: Sixteen patients with a diagnosis of Stargardt disease and a Gly1961Glu mutation were enrolled. All patients underwent a complete ocular examination including best corrected visual acuity, Goldmann visual field (GVF), and...

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Source

Identifiers

PMID: 19578016
DOI: 10.1167/iovs.09-3611

Genes

ABCA4
ERG

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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