Human Connexin 30 (GJB6), a Candidate Gene for Nonsyndromic Hearing Loss: Molecular Cloning, Tissue-Specific Expression, and Assignment to Chromosome 13q12

1999/12/01 by Philip M. Kelley, Satoko Abe, James W. Askew +4 · 44 citations
Biochemistry, Genetics and Molecular Biology · Neuroscience · #Audiology #Biology #Connexin #Connexins and lens biology #Gap junction #Gene #Genetics #Hearing Loss and Rehabilitation #Hearing loss #Hearing, Cochlea, Tinnitus, Genetics #Molecular biology #Mutation

paper · doi:10.1006/geno.1999.6002

published in Genomics 62(2), 172-176 (Elsevier BV)

crossref issued 1999/12/01 · crossref published 1999/12/01 · crossref published-print 1999/12/01 · openalex publication_date 1999/12/01 · crossref created 2002/10/07 · crossref deposited 2019/05/07 · openalex created_date 2025/10/10 · crossref indexed 2026/03/07 · openalex updated_date 2026/06/24

Citations

• Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
• Expression of the gap-junction connexins 26 and 30 in the rat cochlea
• Basic local alignment search tool
• Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

Cited by

• A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews
• A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment
• A large deletion including most of GJB6 in recessive non syndromic deafness: a digenic effect?
• A Novel Connexin 30 Mutation in Clouston Syndrome
• GJB6 [wikipedia]