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Summary Anatomy Item Literature (284) Expression Attributions Wiki
XB-ANAT-221

Papers associated with otic placode (and gjb2)

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RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM(®) genes for hereditary disorders of hearing and balance., Ramírez-Gordillo D., BMC Res Notes. November 18, 2015; 8 691.      

The human Cx26-D50A and Cx26-A88V mutations causing keratitis-ichthyosis-deafness syndrome display increased hemichannel activity., Mhaske PV., Am J Physiol Cell Physiol. June 15, 2013; 304 (12): C1150-8.

Zebrafish cx30.3: identification and characterization of a gap junction gene highly expressed in the skin., Tao L., Dev Dyn. October 1, 2010; 239 (10): 2627-36.

Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss., Meşe G., Hum Genet. August 1, 2004; 115 (3): 191-9.

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