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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
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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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2014
2014
ZEBRAFISH AS A MODEL FOR DETERMINING THE MECHANISMS CAUSING DEAFNESS IN MYH9-RELATED DISEASE by Luke Spychalla The University of… 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
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2006
2006
Multiple mouse embryonic stem (ES) cell banks expand the capability to characterize functions of genes implicated in human… Expand
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2006
2006
Background: Nonsyndromic autosomal‐dominant, adult‐onset sensorineural hearing loss resulting from DFNA17 was described in a… Expand
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2002
2002
 
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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
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