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DEAFNESS, AUTOSOMAL DOMINANT 23

Known as: DFNA23 
National Institutes of Health

Related topics

Related topics

3 relations
Autosomal dominant inheritanceSIX1, 3-BP DEL, 397GGA

Broader (1)

Sensorineural Hearing Loss (disorder)

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2005
2005
A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12
Background: Non-syndromic hearing loss is among the most genetically heterogeneous traits known in humans. To date, at least 50… 
2003
2003
A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1–14q24.3 in large consanguineous kindred from Pakistan
Autosomal recessive nonsyndromic deafness is one of the most frequent forms of inherited hearing impairment. Over 30 autosomal… 
2000
2000
A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindred.
DFNA23, a novel locus for autosomal dominant nonsyndromic hearing loss, was identified in a Swiss German kindred. DNA samples… 
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