Voltage opens unopposed gap junction hemichannels formed by a connexin 32 mutant associated with X-linked Charcot-Marie-Tooth disease
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference51 articles.
1. Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease
2. Connexin32 is a myelin-related protein in the PNS and CNS
3. Altered gene expression in Schwann cells of connexin32 knockout animals
4. Changes in Permeability Caused by Connexin 32 Mutations Underlie X-Linked Charcot-Marie-Tooth Disease
5. Isoform Composition of Connexin Channels Determines Selectivity among Second Messengers and Uncharged Molecules
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