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Stargardt disease 4

Known as: STGD4 
National Institutes of Health

Related topics

Related topics

1 relation

Broader (1)

Age related macular degeneration

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Prominin-1 Is a Novel Regulator of Autophagy in the Human Retinal Pigment Epithelium
Purpose Prominin-1 (Prom1) is a transmembrane glycoprotein, which is expressed in stem cell lineages, and has recently been… 
2009
2009
Clinical features and linkage analysis for a Chinese family with autosomal dominant central areolar choroidal dystrophy.
BACKGROUND A Chinese family with autosomal dominant central areolar choroidal dystrophy (CACD) was identified. The purpose of… 
Highly Cited
1999
Highly Cited
1999
A new locus for autosomal dominant stargardt-like disease maps to chromosome 4.
Stargardt disease (STGD) is the most common hereditary macular dystrophy and is characterized by decreased central vision… 
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