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Voltage opens unopposed gap junction hemichannels formed by a connexin 32 mutant associated with X-linked Charcot-Marie-Tooth disease

The X-linked form of Charcot-Marie-Tooth disease (CMTX) is an inherited peripheral neuropathy that arises in patients with mutations in the gene encoding the gap junction protein connexin 32 (Cx32), which is expressed by Schwann cells. We recently showed that Cx32 containing the CMTX-associated muta...

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Detalhes bibliográficos
Main Authors: Abrams, C. K., Bennett, M. V. L., Verselis, V. K., Bargiello, T. A.
Formato: Artigo
Idioma:Inglês
Publicado em: The National Academy of Sciences 2002
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC122634/
https://ncbi.nlm.nih.gov/pubmed/11891346
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.261713499
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