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Deafness, Autosomal Dominant 13

Known as: DFNA13 
 
National Institutes of Health

Papers overview

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2016
2016
OBJECTIVES Mutations in EYA4 can cause nonsyndromic autosomal dominant sensorineural hearing impairment (DFNA10) or a syndromic… Expand
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2016
2016
La mutagenese chimique aleatoire par l’Ethyl-Nitroso-Uree (ENU), dont la puissance a ete largement demontree au cours de ces… Expand
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2014
2014
OBJECTIVES Recently, OTOG and OTOGL were identified as human deafness genes. Currently, only four families are known to have… Expand
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2012
2012
OBJECTIVE To evaluate hearing impairment and cochlear function in non-ocular Stickler syndrome. STUDY DESIGN Multifamily study… Expand
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2009
2009
Temporal processing, frequency discrimination and frequency resolution, three basic mechanisms involved in speech perception… Expand
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2007
2007
An autosomal dominant inherited disorder known as DFNA8/12 causes mild-tomoderate/severe midfrequency or mild-to-severe… Expand
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2001
2001
Transgenic mice were prepared by homologous recombination with a Col11a2 targeting gene in which an inverted neomycin-resistant… Expand
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2001
2001
We present a Dutch family with autosomal dominantly inherited mid-frequency and high-frequency sensorineural hearing impairment… Expand
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Highly Cited
1999
Highly Cited
1999
We report that mutation of COL11A2 causes deafness previously mapped to the DFNA13 locus on chromosome 6p. We found two families… Expand
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