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Kidney Int. 2000 Mar;57(3):780-6.

Molecular mechanisms of ion conduction in ClC-type chloride channels: lessons from disease-causing mutations.

Author information

  • Department of Pharmacology, Vanderbilt University, Nashville, Tennessee, USA. chfahlke@physiology.rwth-aachen.de

Abstract

The muscle Cl- channel, ClC-1, is a member of the ClC family of voltage-gated Cl- channels. Mutations in CLCN1, the gene encoding this channel, cause two forms of inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant myotonia (Thomsen). The functional characterization of these naturally occurring mutations not only allowed a better understanding of the pathophysiology of myotonia, it also provided important insights into the structure and function of the entire ClC channel family. This review describes recent experiments using a combination of cellular electrophysiology, molecular genetics, and recombinant DNA technology to study the molecular basis of ion permeation and selection in ClC-type chloride channels.

PMID:
10720929
[PubMed - indexed for MEDLINE]
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