Compound mutations in human anion exchanger 1 are associated with complete distal renal tubular acidosis and hereditary spherocytosis

Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane

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Function of WW Domains as Phosphoserine- or Phosphothreonine-Binding Modules

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The prolyl isomerase Pin1 regulates amyloid precursor protein processing and amyloid-β production

Lucia Pastorino, Anyang Sun, Pei‐Jung Lu et al. · Nature · 2006 · 492 citations

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Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene.

Lesley J. Bruce, Diane L. Cope, Graham K. Jones et al. · Journal of Clinical Investigation · 1997 · 363 citations · Full text

Medicine, Genetics, Molecular Genetics +16