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OTOA gene

Known as: CT108, cancer/testis antigen 108, OTOA 
 
National Institutes of Health

Papers overview

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2017
2017
Hearing impairment (HI) is genetically heterogeneous which hampers genetic counseling and molecular diagnosis. Testing of several… Expand
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Highly Cited
2014
Highly Cited
2014
BackgroundCopy number variants (CNVs) are a well-recognized cause of genetic disease; however, methods for their identification… Expand
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2012
2012
The mechanisms of central auditory processing involved in auditory/vestibular injuries and subsequent tinnitus and hearing loss… Expand
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2012
2012
The gene causative for the human nonsyndromic recessive form of deafness DFNB22 encodes otoancorin, a 120-kDa inner ear-specific… Expand
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Highly Cited
2010
Highly Cited
2010
In communities with high rates of consanguinity and consequently high prevalence of recessive phenotypes, homozygosity mapping… Expand
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Highly Cited
2008
Highly Cited
2008
BackgroundMesothelin is a 40 kDa protein present on the surface of normal mesothelial cells and overexpressed in many human… Expand
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2005
2005
Recessively inherited phenotypes are frequent in the Palestinian population, as the result of a historical tradition of marriages… Expand
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Highly Cited
2002
Highly Cited
2002
A 3,673-bp murine cDNA predicted to encode a glycosylphosphatidylinositol-anchored protein of 1,088 amino acids was isolated… Expand
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2002
2002
BackgroundInteraction between hair cells and acellular gels of the mammalian inner ear, the tectorial and otoconial membranes, is… Expand
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1992
1992
Ly-6A/E molecules were originally implicated in regulation of T cell activation because anti-Ly-6A/E mAb induce IL-2 production… Expand
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