DEAFNESS, AUTOSOMAL DOMINANT 25 (disorder)

Known as: DFNA25, Deafness, Autosomal Dominant 25 
 
National Institutes of Health

Papers overview

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2016
2016
BackgroundOne of the causes of sensorineural hearing loss (SNHL) is degeneration of the inner hair cells in the organ of Corti in… (More)
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2015
2015
Le glutamate est accumule dans des vesicules synaptiques par des transporteurs vesiculaires du glutamate appeles VGLUT1-3. VGLUT1… (More)
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Highly Cited
2008
Highly Cited
2008
Autosomal-dominant sensorineural hearing loss is genetically heterogeneous, with a phenotype closely resembling presbycusis, the… (More)
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2003
2003
OBJECTIVES To clinically characterize a family with nonsyndromic sensorineural hearing loss linked to the DFNA25 gene and to… (More)
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2002
2002
We have studied 36 subjects in a large multigenerational Chinese family that is segregating for an autosomal dominant adult onset… (More)
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2001
2001
Using linkage analysis, we identified a novel dominant locus, DFNA25, for delayed-onset, progressive, high-frequency… (More)
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