Structural Abnormalities and Deficient Maintenance of Peripheral Nerve Myelin in Mice Lacking the Gap Junction Protein Connexin 32

Mutations affecting the connexin 32 (Cx32) gene are associated with the X-linked form of the hereditary peripheral neuropathy Charcot–Marie–Tooth disease (CMTX). We show that Cx32-deficient mice develop a late-onset progressive peripheral neuropathy with abnormalities comparable to those associated...

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Detalhes bibliográficos
Publicado no:J Neurosci
Main Authors: Anzini, Patrizia, Neuberg, Dirk H.-H., Schachner, Melitta, Nelles, Eric, Willecke, Klaus, Zielasek, Jürgen, Toyka, Klaus V., Suter, Ueli, Martini, Rudolf
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 1997
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6573343/
https://ncbi.nlm.nih.gov/pubmed/9169515
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.17-12-04545.1997
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