Connexin32 Mutations Cause Loss of Function in Schwann Cells and Oligodendrocytes Leading to PNS and CNS Myelination Defects

The gap junction (GJ) protein connexin32 (Cx32) is expressed by myelinating Schwann cells and oligodendrocytes and is mutated in X-linked Charcot-Marie-Tooth disease. In addition to a demyelinating peripheral neuropathy, some Cx32 mutants are associated with transient or chronic CNS phenotypes. To i...

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Main Authors: Sargiannidou, Irene, Vavlitou, Natalie, Aristodemou, Sophia, Hadjisavvas, Andreas, Kyriacou, Kyriacos, Scherer, Steven S., Kleopa, Kleopas A.
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2009
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2721059/
https://ncbi.nlm.nih.gov/pubmed/19369543
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.0325-09.2009
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