MYO7A gene

Known as: NSRD2, MYOSIN, UNCONVENTIONAL, FAMILY VII, MEMBER A, MYU7A 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1996-2018
05101519962018

Papers overview

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2013
2013
Usher 1 patients are born profoundly deaf and then develop retinal degeneration. Thus they are readily identified before the… (More)
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2009
2009
PURPOSE To study retinal microstructure in Usher Syndrome type 1B (USH1B) caused by MYO7A mutations as a prelude to treatment… (More)
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2008
2008
Usher syndrome (USH) is a genetically heterogeneous group of autosomal recessive deaf-blinding disorders. Pathophysiology leading… (More)
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2008
2008
Recessive mutations of MYO7A, encoding unconventional myosin VIIA, can cause either a deaf-blindness syndrome (type 1 Usher… (More)
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2006
2006
Usher syndrome type I is the most severe form of Usher syndrome. It is an autosomal recessive disorder characterized by profound… (More)
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2004
2004
Usher syndrome type I (USH1), the most severe form of this syndrome, is characterized by profound congenital sensorineural… (More)
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2002
2002
Usher syndrome is an autosomal recessive disorder characterized by congenital hearing impairment and retinitis pigmentosa. Three… (More)
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Highly Cited
2001
Highly Cited
2001
Usher syndrome type I (USH1) is an autosomal recessive disorder characterized by congenital sensorineural hearing loss… (More)
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Highly Cited
2000
Highly Cited
2000
Usher syndrome type 1 (USH1) is an autosomal recessive sensory defect involving congenital profound sensorineural deafness… (More)
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Highly Cited
1997
Highly Cited
1997
Hereditary non-syndromic profound deafness affects about 1 in 2000 children prior to language acquisition. In 80% of the cases… (More)
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