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USH2A protein, human

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

Papers overview

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2015
2015
45 pages. A thesis presented to the Department of Biology and the Clark Honors College of the University of Oregon in partial… Expand
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2010
2010
The transmembrane splice variant of usherin is concentrated in the ankle-link complex of stereocilia in the vertebrate cochlea… Expand
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Highly Cited
2007
Highly Cited
2007
Usher syndrome type IIA (USH2A), characterized by progressive photoreceptor degeneration and congenital moderate hearing loss, is… Expand
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Highly Cited
2005
Highly Cited
2005
Usher syndrome type IIa (USH2A) combines moderate to severe congenital hearing impairment and retinitis pigmentosa. It is the… Expand
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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… Expand
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2003
2003
  • ZM Ahmeda, S Riazuddinb, S Riazuddina, ER Wilcoxa
  • 2003
  • Corpus ID: 38397325
Association of sensorineural deafness and progressive retinitis pigmentosa with and without a vestibular abnormality is the… Expand
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2002
2002
People with Usher's syndrome type IIa have mutations in a novel gene encoding a protein with domains commonly found in many types… Expand
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2002
2002
Usher syndrome is an autosomal recessive disease that results in varying degrees of hearing loss and retinitis pigmentosa. Three… Expand
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