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Deafness, Autosomal Dominant 10

Known as: DFNA10 
 
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
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
Dominant, truncating mutations of eyes absent 4 (EYA4) on chromosome 6q23 can cause either nonsyndromic hearing loss DFNA10 or… Expand
2007
2007
Nonsyndromic autosomal dominant sensorineural hearing loss (SNHL) at the DFNA10 locus was described in two families in 2001… Expand
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
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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Highly Cited
1996
Highly Cited
1996
Late-onset non-syndromic hearing impairment is the most common type of neurological dysfunction in the elderly. It can be either… Expand