We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleNovel mutations in GJB2 encoding connexin-26 in Japanese patients with keratitis-ichthyosis-deafness syndrome.AuthorsYotsumoto, S; Hashiguchi, T; Chen, X; Ohtake, N; Tomitaka, A; Akamatsu, H; Matsunaga, K; Shiraishi, S; Miura, H; Adachi, J; Kanzaki, TAbstractGermline missense mutations in the GJB2 gene that encodes connexin-26 (Cx26) have recently been found to be the cause of the keratitis-ichthyosis-deafness (KID) syndrome.PublicationThe British journal of dermatology, 2003, Vol 148, Issue 4, p649ISSN0007-0963Publication typeJournal ArticleDOI10.1046/j.1365-2133.2003.05245.x