Deafness, Autosomal Recessive 12

Known as: DFNB12 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1996-2018
012319962018

Papers overview

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2011
2011
BACKGROUND Recessive mutant alleles of MYO7A, USH1C, CDH23, and PCDH15 cause non-syndromic deafness or type 1 Usher syndrome… (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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2007
2007
Mutations in the CDH23 gene are known to be responsible for both Usher syndrome type ID (USH1D) and non-syndromic hearing loss… (More)
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Highly Cited
2005
Highly Cited
2005
Mutant alleles of the gene encoding cadherin 23 are associated with Usher syndrome type 1 (USH1D), isolated deafness (DFNB12) in… (More)
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Highly Cited
2004
Highly Cited
2004
oskar messenger RNA localization at the posterior pole of the Drosophila oocyte is essential for germline and abdomen formation… (More)
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Highly Cited
2002
Highly Cited
2002
Usher syndrome type I is characterized by congenital hearing loss, retinitis pigmentosa (RP), and variable vestibular areflexia… (More)
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Highly Cited
2001
Highly Cited
2001
Genes causing nonsyndromic autosomal recessive deafness (DFNB12) and deafness associated with retinitis pigmentosa and vestibular… (More)
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2001
2001
Mutations at the waltzer (v) locus result in deafness and vestibular dysfunction due to degeneration of the neuroepithelium… (More)
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Highly Cited
2001
Highly Cited
2001
Mouse chromosome 10 harbors several loci associated with hearing loss, including waltzer (v), modifier-of deaf waddler (mdfw) and… (More)
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1996
1996
We report here, the localization of a new recessive non-syndromal deafness gene (DFNB12) to 10q21-22 by linkage analysis, of a… (More)
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