https://www.frontiersin.org/journals/cell-and-developmental-biology/articles/10.3389/fcell.2022.1071202/full
Frontiers | Expression of KID syndromic mutation Cx26S17F produces hyperactive hemichannels in...
Some mutations in gap junction (GJ) protein Connexin 26 (Cx26) lead to syndromic deafness, where hearing impairment is associated with skin disease, like in ...
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