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Article

A new locus for autosomal dominant stargardt-like disease maps to chromosome 4.

American journal of human genetics - 1 May 1999

Kniazeva M, Chiang M F, Morgan B, Anduze A L, Zack D J, Han M, Zhang K

Abstract excerpt

Stargardt disease (STGD) is the most common hereditary macular dystrophy and is characterized by decreased central vision, atrophy of the macula and underlying retinal-pigment epithelium, and frequent presence of prominent flecks in the posterior pole of the retina. STGD is most commonly inherite...

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Identifiers

PMID: 10205271
DOI: 10.1086/302377
PMCID: PMC1377876

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-10205271-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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