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Deafness, autosomal dominant nonsyndromic sensorineural 22

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

Papers overview

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2019
2019
Myosin VI is an actin-associated molecular motor vital for auditory and vestibular function. It is encoded by MYO6 located on… Expand
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2018
2018
Autosomal dominant non-syndromic hearing loss (ADNSHL) is characterized by postlingual progressive onset. Due to its high genetic… Expand
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2018
2018
BACKGROUND The MYO6 gene, if altered, can cause nonsyndromic hearing loss (NSHL) either in an autosomal dominant (AD) (DFNA22) or… Expand
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2016
2016
Mutations in myosin VI have been associated with autosomal-recessive (DFNB37) and autosomal-dominant (DFNA22) deafness in humans… Expand
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2014
2014
Autosomal dominant types of nonsyndromic hearing loss (ADNSHL) are typically postlingual in onset and progressive. High genetic… Expand
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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… Expand
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2009
2009
Clinical and audiological examination was done in 2 Belgian families with autosomal dominant sensorineural hearing loss (SNHL… Expand
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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… Expand
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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… Expand
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