Deafness, Autosomal Dominant 13

Known as: DFNA13 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1997-2016
012319972016

Papers overview

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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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Review
2016
Review
2016
Hearing impairment is considered as the most prevalent impairment worldwide. Almost 600 million people in the world suffer from… (More)
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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… (More)
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2012
2012
OBJECTIVE To evaluate hearing impairment and cochlear function in non-ocular Stickler syndrome. STUDY DESIGN Multifamily study… (More)
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2009
2009
Temporal processing, frequency discrimination and frequency resolution, three basic mechanisms involved in speech perception… (More)
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2001
2001
Transgenic mice were prepared by homologous recombination with a Col11a2 targeting gene in which an inverted neomycin-resistant… (More)
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2001
2001
We present a Dutch family with autosomal dominantly inherited mid-frequency and high-frequency sensorineural hearing impairment… (More)
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2001
2001
OBJECTIVE To analyze the phenotype in a 5-generation DFNA13 family with a missense mutation in the COL11A2 gene that causes… (More)
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1997
1997
Nonsyndromic hearing loss (NSHL) is the most common type of hearing impairment in the elderly. Environmental and hereditary… (More)
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