CLC channel function and dysfunction in health and disease
Author:
Publisher
Frontiers Media SA
Subject
Physiology (medical),Physiology
Reference138 articles.
1. Drastic reduction of the slow gate of human muscle chloride channel (ClC-1) by mutation C277S;Accardi;J. Physiol,2001
2. Synergism between halide binding and proton transport in a CLC-type exchanger;Accardi;J. Mol. Biol,2006
3. Secondary active transport mediated by a prokaryotic homologue of ClC Cl- channels;Accardi;Nature,2004
4. Fast and slow gating relaxations in the muscle chloride channel ClC-1;Accardi;J. Gen. Physiol,2000
5. Separate ion pathways in a Cl−/H+ exchanger;Accardi;J. Gen. Physiol,2005
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