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Deafness, Autosomal Dominant 28

Known as: DFNA28 
 
National Institutes of Health

Papers overview

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2017
2017
ObjectiveCongenital fibrosis of the extraocular muscles type 1 (CFEOM1) is known to be caused by mutations in KIF21A or TUBB3 or… Expand
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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… Expand
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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… Expand
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2011
2011
Congenital and progressive hearing impairment is a common distressing disease. The progressive dominant hearing loss DFNA28 in… Expand
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Highly Cited
2002
Highly Cited
2002
We ascertained a large American family with an autosomal dominant form of progressive non-syndromic sensorineural hearing loss… Expand
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