Deafness, autosomal dominant nonsyndromic sensorineural 22

Known as: DFNA 22, DFNA22, Deafness, Autosomal Dominant 22 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2001-2015
01220012015

Papers overview

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2016
2016
Mutations in myosin VI have been associated with autosomal-recessive (DFNB37) and autosomal-dominant (DFNA22) deafness in humans… (More)
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2015
2015
OBJECTIVES To elucidate the involvement of MYO6 mutations, known to be responsible for DFNA22/DFNB37, in Japanese hearing loss… (More)
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2014
2014
Autosomal dominant types of nonsyndromic hearing loss (ADNSHL) are typically postlingual in onset and progressive. High genetic… (More)
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2013
2013
Since deafness is the most common sensorineural disorder in humans, better understanding of the underlying causes is necessary to… (More)
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2013
2013
Mutations in MYO6 encoding an atypical myosin motor protein important for inner ear hair cell function have been associated with… (More)
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2010
2010
Clinical and audiological examination was done in 2 Belgian families with autosomal dominant sensorineural hearing loss (SNHL… (More)
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2008
2008
Hearing loss is the most common sensory disorder, affecting 1 in 650 newborns. Linkage analysis revealed linkage to locus DFNA22… (More)
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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… (More)
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Highly Cited
2003
Highly Cited
2003
Cosegregation of profound, congenital deafness with markers on chromosome 6q13 in three Pakistani families defines a new… (More)
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Highly Cited
2001
Highly Cited
2001
Mutations in the unconventional myosin VI gene, Myo6, are associated with deafness and vestibular dysfunction in the Snell's… (More)
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