Transgenic replacement of Cx32 in gap junction deficient oligodendrocytes rescues the phenotype of a hypomyelinating leukodystrophy model. Schiza N, Sargiannidou I, Kagiava A, Karaiskos C, Nearchou M, Kleopa KA Hum Mol Genet. 2014 Dec 18. PMID: 25524707. Abstract CommentRecommendBookmarkWatch