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Deafness, Autosomal Dominant 10

Known as: DFNA10 
 
National Institutes of Health

Papers overview

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2015
2015
Linkage to an interval overlapping the DFNA10 locus on chromosome 6q22-23 was found through genome wide linkage analysis in a… Expand
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2015
2015
The EYA4 gene encodes a 640-amino-acid protein that serves as a transcription factor. This protein contains a highly conserved… Expand
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2007
2007
Nonsyndromic autosomal dominant sensorineural hearing loss (SNHL) at the DFNA10 locus was described in two families in 2001… Expand
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2007
2007
Dominant, truncating mutations of eyes absent 4 (EYA4) on chromosome 6q23 can cause either nonsyndromic hearing loss DFNA10 or… Expand
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2004
2004
Allele variants of EYA1 and EYA4, two members of the vertebrate Eya gene family, underlie two types of inherited human deafness… Expand
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2002
2002
BackgroundHereditary hearing impairment (HHI) is a heterogeneous class of disorders that shows various patterns of inheritance… Expand
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Highly Cited
2000
Highly Cited
2000
BACKGROUND Dilated cardiomyopathy (DCM) and sensorineural hearing loss (SNHL) are prevalent disorders that occur alone or as… Expand
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2000
2000
OBJECTIVE To report the otologic and audiometric characteristics of a nonsyndromic postlingual sensorineural hearing impairment… Expand
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2000
2000
Abstract. DFNA10 originally was mapped to the long arm of chromosome 6 in a large American family segregating for autosomal… Expand
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1996
1996
Late-onset non-syndromic hearing impairment is the most common type of neurological dysfunction in the elderly. It can be either… Expand
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