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This book reviews a wide variety of congenital and acquired conditions caused by abnormalities in ion-transport mechanisms. It starts with a description of relatively simple channels that respond to voltage changes or certain cellular metabolites by a conformational change that opens the pore. These channels are closed by a cytosolic loop that plugs the pore. The book continues with more complex channels composed of multiple subunits of the same composition and controlled by other subunits with a different composition. The complexity increases in a last group of ion channels that regulate more than one type of ion passage and form
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