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3. Cation transport activity of anion exchanger 1 mutations found in inherited distal renal tubular acidosis. Walsh S; Borgese F; Gabillat N; Unwin R; Guizouarn H Am J Physiol Renal Physiol; 2008 Aug; 295(2):F343-50. PubMed ID: 18524859 [TBL] [Abstract][Full Text] [Related]
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11. Rapid Cl⁻/HCO⁻₃exchange kinetics of AE1 in HEK293 cells and hereditary stomatocytosis red blood cells. Frumence E; Genetet S; Ripoche P; Iolascon A; Andolfo I; Le Van Kim C; Colin Y; Mouro-Chanteloup I; Lopez C Am J Physiol Cell Physiol; 2013 Sep; 305(6):C654-62. PubMed ID: 23842529 [TBL] [Abstract][Full Text] [Related]
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13. Trafficking and folding defects in hereditary spherocytosis mutants of the human red cell anion exchanger. Quilty JA; Reithmeier RA Traffic; 2000 Dec; 1(12):987-98. PubMed ID: 11208088 [TBL] [Abstract][Full Text] [Related]
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