Kir1.1 is an inwardly rectifying potassium channel expessed in kidney, skeletal muscle, liver, pancreas, spleen and the central nervous system. Mutations in Kir1.1 are responsible for Bartter's syndrome (renal salt loss) and hereditary hypertension with hyperkalemia. Kir1.1 has therapeutic potential in treatment of hypertension.
Human Kir1.1 Potassium Channel EZCells™ TT
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