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DEAFNESS, AUTOSOMAL DOMINANT 17

Known as: DFNA17 
National Institutes of Health

Related topics

Related topics

2 relations
Autosomal dominant inheritance

Broader (1)

SEBASTIAN SYNDROME

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family
We studied a family presenting 10 individuals affected by autosomal dominant deafness in all frequencies and three individuals… 
2014
2014
Hereditary hearing impairment. Clinical, genetic and psychophysical aspects of Non-Ocular Stickler syndrome, HDR syndrome, DFNA10, DFNA17 and DFNA60
2006
2006
Cochlear Implants for DFNA17 Deafness
Background: Nonsyndromic autosomal‐dominant, adult‐onset sensorineural hearing loss resulting from DFNA17 was described in a… 
2006
2006
Absence of hearing loss in a mouse model for DFNA17 and MYH9-related disease: The use of public gene-targeted ES cell resources
2002
2002
Auditory phenotype of DFNA17.
Review
1999
Review
1999
Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes.
This review is concerned with the present state of phenotypical characterization of known genotypes of non-syndromal autosomal… 
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