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DEAFNESS, AUTOSOMAL DOMINANT 17

Known as: DFNA17 
National Institutes of Health

Papers overview

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2015
2015
MYH9‐related disease (MYH9‐RD) is a rare autosomal dominant disease caused by mutation of MYH9, the gene encoding for the heavy… Expand
2014
2014
We studied a family presenting 10 individuals affected by autosomal dominant deafness in all frequencies and three individuals… Expand
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2008
2008
Autosomal dominant inheritance is described in about 20% of all nonsyndromic hearing loss with currently 54 distinct loci (DFNA1… Expand
2006
2006
Background: Nonsyndromic autosomal‐dominant, adult‐onset sensorineural hearing loss resulting from DFNA17 was described in a… Expand
2006
2006
Multiple mouse embryonic stem (ES) cell banks expand the capability to characterize functions of genes implicated in human… Expand
2002
2002
Highly Cited
2001
Highly Cited
2001
May-Hegglin anomaly (MHA) and Fechtner (FTNS) and Sebastian (SBS) syndromes are autosomal dominant platelet disorders that share… Expand
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Highly Cited
2000
Highly Cited
2000
The authors had previously mapped a new locus-DFNA17, for nonsyndromic hereditary hearing impairment-to chromosome 22q12.2-q13. 3… Expand