Pathogenesis of X-Linked Charcot-Marie-Tooth Disease: Differential Effects of Two Mutations in Connexin 32

X-Linked Charcot-Marie-Tooth disease is an inherited peripheral neuropathy arising in patients with mutations in the gene encoding connexin 32 (Cx32). Cx32 is expressed at the paranodes and Schmidt-Lantermann incisures of myelinating Schwann cells in which it is believed to form a reflexive pathway...

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Detalhes bibliográficos
Publicado no:J Neurosci
Main Authors: Abrams, Charles K., Freidin, Mona, Bukauskas, Feliksas, Dobrenis, Kostantin, Bargiello, Thaddeus A., Verselis, Vytas K., Bennett, Michael V. L., Chen, Lei, Sahenk, Zarife
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2003
Assuntos:
Cellular/Molecular
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4513672/
https://ncbi.nlm.nih.gov/pubmed/14627639
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.23-33-10548.2003
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