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GJB4 gene

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

Papers overview

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2016
2016
Dear Editor, Erythrokeratodermia variabilis (EKV) is a rare autosomal dominant inherited skin disorder characterized by migratory… Expand
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2015
2015
OBJECTIVE To investigate the association of eight connexin genes (GJB2, GJB4, GJA1P1, GJB6, GJB3, GJA1, GJB1, and GJC3) and the… Expand
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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… Expand
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2012
2012
 
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2011
2011
BACKGROUND Progressive symmetrical erythrokeratodermia (PSEK) is a rare inherited cornification disorder characterized by… Expand
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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… Expand
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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… Expand
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Highly Cited
2003
Highly Cited
2003
Erythrokeratodermia variabilis is an autosomal dominant genodermatosis characterized by persistent plaque-like or generalized… Expand
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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… Expand
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