Deafness, Autosomal Dominant 10

Known as: DFNA10 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1996-2015
012319962015

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2016
2016
OBJECTIVES Mutations in EYA4 can cause nonsyndromic autosomal dominant sensorineural hearing impairment (DFNA10) or a syndromic… (More)
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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… (More)
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2007
2007
Nonsyndromic autosomal dominant sensorineural hearing loss (SNHL) at the DFNA10 locus was described in two families in 2001… (More)
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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… (More)
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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… (More)
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2002
2002
BACKGROUND Hereditary hearing impairment (HHI) is a heterogeneous class of disorders that shows various patterns of inheritance… (More)
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2000
2000
OBJECTIVE To report the otologic and audiometric characteristics of a nonsyndromic postlingual sensorineural hearing impairment… (More)
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2000
2000
BACKGROUND Dilated cardiomyopathy (DCM) and sensorineural hearing loss (SNHL) are prevalent disorders that occur alone or as… (More)
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2000
2000
DFNA10 originally was mapped to the long arm of chromosome 6 in a large American family segregating for autosomal dominant… (More)
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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… (More)
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