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Blood|July 1, 1997
Modulation of clinical expression and band 3 deficiency in hereditary spherocytosisN Alloisio, P Texier, A Vallier, et al.
Journal of Molecular Biology|February 20, 1992
Basis of unique red cell membrane properties in hereditary ovalocytosisA E Schofield, M J Tanner, J C Pinder, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 1998
Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosisF E Karet, F J Gainza, A Z Györy, et al.
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