Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

DEAFNESS, AUTOSOMAL DOMINANT 23

Known as: DFNA23 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2006
2006
Background: Non-syndromic hearing loss is among the most genetically heterogeneous traits known in humans. To date, at least 50… Expand
  • table 1
  • table 2
Is this relevant?
2003
2003
Autosomal recessive nonsyndromic deafness is one of the most frequent forms of inherited hearing impairment. Over 30 autosomal… Expand
  • figure 1
  • table 1
Is this relevant?
2000
2000
DFNA23, a novel locus for autosomal dominant nonsyndromic hearing loss, was identified in a Swiss German kindred. DNA samples… Expand
Is this relevant?