COCH gene

Known as: COCH, COCH-5B2, COCH5B2 
 
National Institutes of Health

Papers overview

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Review
2009
Review
2009
Hearing impairment is the most common sensory disorder, present in 1 of every 500 newborns. With 46 genes implicated in… (More)
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2005
2005
Dominant progressive hearing loss and vestibular dysfunction DFNA9 is caused by mutations of the human COCH gene. COCH encodes… (More)
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2003
2003
The COCH gene is the only gene identified in man that causes autosomal dominantly inherited hearing loss associated with… (More)
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2001
2001
Missense mutations in the COCH gene, which is expressed preferentially at high levels in the inner ear, cause the autosomal… (More)
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Highly Cited
2000
Highly Cited
2000
The compound leaf primordium of pea represents a marginal blastozone that initiates organ primordia, in an acropetal manner, from… (More)
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1999
1999
We analysed a Dutch family with autosomal dominant non-syndromic progressive sensorineural hearing loss and mapped the underlying… (More)
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1999
1999
We report the genetic analysis of one large Belgian and two small Dutch families with autosomal dominant non-syndromic… (More)
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Highly Cited
1998
Highly Cited
1998
DFNA9 is an autosomal dominant, nonsyndromic, progressive sensorineural hearing loss with vestibular pathology. Here we report… (More)
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1997
1997
Previously we identified a partial human cDNA for a novel cochlear transcript, hCoch-5B2 (HGMW-approved symbol D14S564E), using… (More)
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Highly Cited
1994
Highly Cited
1994
We used a combination of subtractive hybridization and differential screening strategies to identify genes that may function… (More)
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