Cochlear connexin 30 homomeric and heteromeric channels exhibit distinct assembly mechanisms
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DOI: 10.1016/j.mod.2018.10.001
Abstract: Many of the mutations in GJB2 and GJB6, which encode connexins 26 and 30 (Cx26 and Cx30), impair the formation of membrane channels and cause autosomal syndromic and non-syndromic hearing loss. In cochlear non-sensory supporting… read more here.
Keywords: homomeric heteromeric; distinct assembly; exhibit distinct; heteromeric gap ... See more keywords