USH2A protein, human

Known as: usherin, Usher syndrome 2A (autosomal recessive, mild) protein, human, Usher syndrome 2A protein, human 
 
National Institutes of Health

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Topic mentions per year

2002-2011
0120022011

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2011
2011
INTRODUCTION Usher syndrome is a disorder characterized by progressive retinitis pigmentosa, prelingual sensory hearing loss and… (More)
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2007
Highly Cited
2007
Usher syndrome type IIA (USH2A), characterized by progressive photoreceptor degeneration and congenital moderate hearing loss, is… (More)
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2005
2005
Usher syndrome is a genetically heterogeneous disorder characterized by hearing loss with retinitis pigmentosa. Usher syndrome… (More)
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2004
2004
Usherin is a basement membrane protein encoded by the gene associated with Usher syndrome type IIa, the most common deaf/blind… (More)
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2002
2002
Usher syndrome is an autosomal recessive disorder characterized by congenital hearing impairment and retinitis pigmentosa. Three… (More)
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