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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… 
Review
2015
Review
2015
The two most common vestibular disorders are motion sickness and vestibular migraine, affecting 30 and 1–2 % of the population… 
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… 
Highly Cited
2011
Highly Cited
2011
Congenital and progressive hearing impairment is a common distressing disease. The progressive dominant hearing loss DFNA28 in… 
Highly Cited
2002
Highly Cited
2002
We ascertained a large American family with an autosomal dominant form of progressive non-syndromic sensorineural hearing loss…