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TECTA wt Allele

Known as: DFNB21, DFNA8, Tectorin, Alpha Gene 
Human TECTA wild-type allele is located within 11q22-q24 and is approximately 90 kb in length. This allele, which encodes alpha-tectorin protein, is… Expand
National Institutes of Health

Papers overview

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2016
2016
BACKGROUND Autosomal recessive non-syndromic hearing loss (ARNSHL) is the most common hereditary form of deafness, and exhibits a… Expand
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2004
2004
BACKGROUND Alpha-tectorin is a noncollagenous component of the tectorial membrane which plays an essential role in auditory… Expand
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2003
2003
enetic factors are thought to account for approximately one half of cases of childhood hearing loss, the majority of which is non… Expand
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2000
2000
In this study, a non-syndromic progressive bilateral high frequency hearing loss is described in a family with 141 identified… Expand
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1999
1999
Abstract. The human α-tectorin (TECTA) gene has recently been cloned and proposed to be involved in autosomal dominant non… Expand
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1999
1999
A gene responsible for autosomal dominant non-syndromic hearing impairment in two families (DFNA8 and DFNA12) has recently been… Expand
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1999
1999
Kristien Verhoeven et al. Nature Genet. 19, 60–62 (1998). The nucleotide numbering of the mouse gene was used for the human… Expand
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1998
1998
We investigated a Swedish family with nonsyndromic progressive bilateral sensorineural hearing loss. Thirteen candidate loci for… Expand
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Highly Cited
1998
Highly Cited
1998
The tectorial membrane is an extracellular matrix of the inner ear that contacts the stereocilia bundles of specialized sensory… Expand
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1998
1998
The tectorial membrane is an extracellular matrix of the inner ear that contacts the stereocilia bundles of specialized sensory… Expand
Is this relevant?