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Mutations in Cx30 that are linked to skin disease and non-syndromic hearing loss exhibit several distinct cellular

Amy C Berger1, John J Kelly, Patrick Lajoie

  • 1Department of Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada.

Journal of Cell Science
|February 14, 2014
PubMed

Keywords:
Bart-Pumphrey syndromeClouston syndromeConnexinGap junctionHearing lossHemichannelKeratitis-ichthyosis-deafness syndromeMutationSkin diseaseVohwinkel syndrome

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