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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
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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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