CDH23 wt Allele

Known as: KIAA1774, KIAA1812, MGC102761 
Human CDH23 wild-type allele is located in the vicinity of 10q22.1 and is approximately 419 kb in length. This allele, which encodes cadherin-23… (More)
National Institutes of Health

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1998-2018
012319982018

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2013
2013
The Cdh23(erl/erl) mice are a novel mouse model for DFNB12 and are characterized by progressive hearing loss. In this study… (More)
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2011
2011
Usher syndrome (USH) is an autosomal recessive disease characterized by hearing loss, retinitis pigmentosa (RP), and, in some… (More)
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2011
2011
Mutations in the human cadherin 23 (CDH23) gene cause deafness, neurosensory, autosomal recessive 12 (DFNB12) nonsyndromic… (More)
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2009
2009
Deafness is the most common form of sensory impairment in humans and is frequently caused by single gene mutations. Interestingly… (More)
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2004
2004
OBJECTIVE To describe the findings of audiovestibular and ophthalmologic examinations in four families with mutations in the… (More)
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2002
2002
 
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2001
2001
The terminal sequences of long cDNAs from human brains were subjected to an improved method of motif-trap screening. This process… (More)
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2001
2001
Usher syndrome (USH) is characterised by hearing impairment and progressive pigmentary retinopathy. USH can be divided into three… (More)
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2000
2000
Usher syndrome type I is an autosomal recessive disorder marked by hearing loss, vestibular areflexia, and retinitis pigmentosa… (More)
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Review
2000
Review
2000
 
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