Deafness, Autosomal Dominant 28

Known as: DFNA28 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2002-2017
01220022017

Papers overview

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2017
2017
Congenital fibrosis of the extraocular muscles type 1 (CFEOM1) is known to be caused by mutations in KIF21A or TUBB3 or other… (More)
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2015
2015
EYA4 and GRHL2 encode transcription factors that play an important role in regulating many developmental stages. Since EYA4 and… (More)
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Review
2015
Review
2015
The two most common vestibular disorders are motion sickness and vestibular migraine, affecting 30 and 1–2 % of the population… (More)
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2013
2013
More than 10 years ago, a c.1609_1610insC mutation in the grainyhead-like 2 (GRHL2) gene was identified in a large family with… (More)
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2011
2011
Congenital and progressive hearing impairment is a common distressing disease. The progressive dominant hearing loss DFNA28 in… (More)
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2002
2002
We ascertained a large American family with an autosomal dominant form of progressive non-syndromic sensorineural hearing loss… (More)
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