GJB4 gene

Known as: CX30.3, GJB4, gap junction protein beta 4 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2002-2015
0120022015

Papers overview

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2015
2015
Numerous studies have confirmed that gap junctions, composed of connexin (Cx) protein, are essential for auditory function… (More)
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2013
2013
OBJECTIVE Autosomal recessive non-syndromic hearing loss (ARNSHL) can be caused by many genes. However, mutations in the GJB2… (More)
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2010
2010
The crucial role of gap junctions, which are composed of connexin (CX) protein, in auditory functions has been confirmed by… (More)
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2010
2010
Mutations of the GJB4 gene, encoding connexin 30.3 (CX30.3), are associated with skin disorders. Recently, this gene was also… (More)
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2009
2009
Noise-induced hearing loss (NIHL) is one of the leading occupational health risks in industrialized countries. It results from an… (More)
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2002
2002
Mutations in GJB1, GJB2, GJB3 and GJB6 are involved in hearing impairment. GJB2, GJB3 and GJB6 are also mutated in patients with… (More)
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