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Deafness, Autosomal Recessive 12

Known as: DFNB12 
 
National Institutes of Health

Papers overview

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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… Expand
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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… Expand
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Highly Cited
2009
Highly Cited
2009
Deafness is the most common form of sensory impairment in humans and is frequently caused by single gene mutations. Interestingly… Expand
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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… Expand
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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… Expand
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2002
2002
Abstract. We have ascertained a multi-generation family with apparent autosomal recessive non-syndromic childhood hearing loss… Expand
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2002
2002
 
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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… Expand
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Highly Cited
2001
Highly Cited
2001
Mutations at the waltzer (v) locus result in deafness and vestibular dysfunction due to degeneration of the neuroepithelium… Expand
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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… Expand
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