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Article

New Treatments for Stargardt Disease and Related Retinal Degenerative Diseases.

Nippon Ganka Gakkai zasshi - 1 Jan 2017

Arai Eisuke, Maeda Akiko, Murakami Akira

Abstract excerpt

Stargardt disease is a progressive hereditary retinal disease which is currently incurable. Although ABCA4 has been identified as a major causative gene, patients with genetic mutations in other genes (PRPH2, ELOVL4, and PROM1) display similar clinical phenotypes as Stargardt disease. Recent advances in genetic and molecular studies have greatly enhanced our understanding of the disease and have led to...

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Source

Identifiers

PMID: 30079717

Genes

ABCA4
ELOVL4
PROM1
PRPH2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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