Transgenic replacement of Cx32 in gap junction-deficient oligodendrocytes rescues the phenotype of a hypomyelinating leukodystrophy model

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Authors: N. Schiza, I. Sargiannidou, A. Kagiava, C. Karaiskos, M. Nearchou, K. A. Kleopa

Journal title: Human Molecular Genetics

Journal number: 09646906

Journal publisher: Oxford University Press

Published year: 2015

Published pages: 2049-2064

DOI identifier: 10.1093/hmg/ddu725

ISSN: 0964-6906