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Chloride channel protein ClC-2 is a voltage-gated chloride ion channel encoded by the CLCN2 gene. It is a member of the CLC family of chloride channels and transporters, which are involved in the regulation of membrane potential, cell volume, and transepithelial transport. Mutations or dysfunctions in ClC–2 have been linked to several human diseases, including epilepsy and megalencephalic leukoencephalopathy with subcortical cysts.
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