An essential role of MAG in mediating axon-myelin attachment in Charcot-Marie-Tooth 1A disease

Charcot-Marie-Tooth disease type 1A (CMT1A) is a hereditary demyelinating peripheral neuropathy caused by the duplication of the PMP22 gene. Demyelination precedes the occurrence of clinical symptoms that correlate with axonal degeneration. It was postulated that a disturbed axon-glia interface cont...

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Main Authors: Kinter, Jochen, Lazzati, Thomas, Schmid, Daniela, Zeis, Thomas, Erne, Beat, Lützelschwab, Roland, Steck, Andreas J., Pareyson, Davide, Peles, Elior, Schaeren-Wiemers, Nicole
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3612363/
https://ncbi.nlm.nih.gov/pubmed/22940629
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2012.08.009
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