Altered CO2 sensitivity of connexin26 mutant hemichannels in vitro
Author:
Affiliation:
1. School of Life Sciences; University of Warwick; Coventry United Kingdom
Funder
Leverhulme Trust
Publisher
Wiley
Subject
Physiology (medical),Physiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.14814/phy2.13038/fullpdf
Reference50 articles.
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2. A novel dominant and a de novo mutation in the GJB2 gene (connexin-26) cause keratitis-ichthyosis-deafness syndrome: implication for cochlear implantation.;Arndt;Otol. Neurotol.,2010
3. Impaired permeability to Ins(1,4,5)P3 in a mutant connexin underlies recessive hereditary deafness;Beltramello;Nat. Cell Biol.,2005
4. Pathogenetic role of the deafness-related M34T mutation of Cx26;Bicego;Hum. Mol. Genet.,2006
5. Hearing loss: frequency and functional studies of the most common connexin26 alleles;D'Andrea;Biochem. Biophys. Res. Commun.,2002
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