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Stargardt disease 4

Known as: STGD4 
National Institutes of Health

Papers overview

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2018
2018
Purpose Stargardt disease (STGD) is the most common form of inherited juvenile macular degeneration. It is inherited as autosomal… Expand
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2017
2017
Purpose Prominin-1 (Prom1) is a transmembrane glycoprotein, which is expressed in stem cell lineages, and has recently been… Expand
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2012
2012
This thesis describes the genetic analysis conducted to investigate the cause of six autosomal dominant macular dystrophies… Expand
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2009
2009
BACKGROUND A Chinese family with autosomal dominant central areolar choroidal dystrophy (CACD) was identified. The purpose of… Expand
Highly Cited
1999
Highly Cited
1999
Stargardt disease (STGD) is the most common hereditary macular dystrophy and is characterized by decreased central vision… Expand
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