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Chloride channel protein 1 (ClC-1) is a voltage-gated chloride channel primarily expressed in skeletal muscle. It plays a crucial role in maintaining the resting membrane potential and regulating muscle excitability. ClC-1 forms a homodimeric structure, with each subunit containing its own ion-conducting pore. Mutations in the CLCN1 gene, encoding ClC-1, lead to myotonia congenita, a condition characterized by delayed muscle relaxation. The channel's function is essential for proper muscle contraction and relaxation cycles.
Modulation of chloride ion conductance through the channel
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