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t/gene-gjb3

GJB3 gene

Discuss publications and research concerning the GJB3 gene.

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Related literature

Establishment of a Gene Detection System for Hotspot Mutations of Hearing Loss.
GJB3
Application of gene detection technique in the antenatal diagnosis of hereditary hearing loss.
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[Identification of novel common mutations among patients with non-syndromic hearing loss with high-throughput gene capture technology].
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[Screening of mutations of deafness-related genes in women of child-bearing age from Shijiazhuang area].
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Erythrokeratodermia variabilis et progressiva.
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Deafness gene mutations in newborns in Beijing.
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Evaluation of the pathogenicity of GJB3 and GJB6 variants associated with nonsyndromic hearing loss.
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Erythrokeratoderma variabilis caused by a recessive mutation in GJB3.
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Novel and recurrent connexin 30.3 and connexin 31 mutations associated with erythrokeratoderma variabilis.
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GJB2 mutations in patients with nonsyndromic hearing loss from Croatia.
GJB3

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