Impaired Differentiation of Schwann Cells in Transgenic Mice with Increased PMP22 Gene Dosage

An intrachromosomal duplication containing the PMP22gene is associated with the human hereditary peripheral neuropathy Charcot-Marie-Tooth disease type 1A, and PMP22 overexpression as a consequence of increased PMP22 gene dosage has been suggested as causative event in this frequent disorder of peri...

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Detalhes bibliográficos
Publicado no:J Neurosci
Main Authors: Magyar, Josef P., Martini, Rudolf, Ruelicke, Thomas, Aguzzi, Adriano, Adlkofer, Katrin, Dembic, Zlatko, Zielasek, Jürgen, Toyka, Klaus V., Suter, Ueli
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 1996
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6578876/
https://ncbi.nlm.nih.gov/pubmed/8757248
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.16-17-05351.1996
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