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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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2020
2020
The contribution of GJB4 and GJC3 gene variants to hearing impairment in Africa has not yet been studied. Here, we investigated… Expand
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2016
2016
was treated with a recombinant growth hormone until adolescence, which resulted in her reaching the height of 153 cm. Until she… Expand
2015
2015
OBJECTIVE To investigate the association of eight connexin genes (GJB2, GJB4, GJA1P1, GJB6, GJB3, GJA1, GJB1, and GJC3) and the… Expand
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
Figure 2. (a) c.403C>G mutation in GJB3 in proband of family 2. (b) Wild-type sequence of corresponding part in GJB3. Dear Editor… Expand
2011
2011
Background.  Progressive symmetrical erythrokeratodermia (PSEK) is a rare inherited cornification disorder characterized by… Expand
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
Highly Cited
2003
Highly Cited
2003
Erythrokeratodermia variabilis is an autosomal dominant genodermatosis characterized by persistent plaque-like or generalized… Expand
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