STRC gene

Known as: STEREOCILIN, STRC 
 
National Institutes of Health

Papers overview

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2017
2017
OBJECTIVE This study aimed to clarify the molecular epidemiology of hearing loss by identifying the responsible genes in patients… (More)
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2016
2016
OBJECTIVE Copy number variations (CNVs), a major cause of genetic hearing loss, most frequently involve the STRC gene, located on… (More)
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2015
2015
Increasing attention has been directed toward assessing mutational fallout of stereocilin (STRC), the gene underlying DFNB16. A… (More)
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2014
2014
Next-generation sequencing (NGS) technologies have revolutionized genetic testing by enabling simultaneous analysis of… (More)
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2012
2012
Hearing loss is the most prevalent sensory perception deficit in humans, affecting 1/500 newborns, can be syndromic or… (More)
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2011
2011
The tectorial membrane (TM) is an extracellular matrix of the cochlea whose prominent role in hearing has been demonstrated… (More)
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2011
2011
Stereocilin is defective in a recessive form of deafness, DFNB16. We studied the distribution of stereocilin in the developing… (More)
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Highly Cited
2008
Highly Cited
2008
Although the cochlea is an amplifier and a remarkably sensitive and finely tuned detector of sounds, it also produces conspicuous… (More)
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Highly Cited
2003
Highly Cited
2003
In the course of positional cloning of the Congenital Dyserythropoietic Anemia type I (CDAI) [MIM 224120] gene on 15q15.1–15.3… (More)
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Highly Cited
2001
Highly Cited
2001
Hearing impairment affects about 1 in 1,000 children at birth. Approximately 70 loci implicated in non-syndromic forms of… (More)
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