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...

Description complète

Enregistré dans:
Détails bibliographiques
Publié dans:J Neurosci
Auteurs principaux: Anzini, Patrizia, Neuberg, Dirk H.-H., Schachner, Melitta, Nelles, Eric, Willecke, Klaus, Zielasek, Jürgen, Toyka, Klaus V., Suter, Ueli, Martini, Rudolf
Format: Artigo
Langue:Inglês
Publié: Society for Neuroscience 1997
Sujets:
Articles
Accès en ligne: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
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires