Author:
Eber Stefan W.,Gonzalez Jennifer M.,Lux Marcia L.,Scarpa Alphonse L.,Tse William T.,Dornwell Marion,Herbers Jutta,Kugler Wilfried,Ozcan Refik,Pekrun Arnulf,Gallagher Patrick G.,Schroter Werner,Forget Bernard G.,Lux Samuel E.
Publisher
Springer Science and Business Media LLC
Reference35 articles.
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2. Pekrun, A., Eber, S.W., Kuhlmey, A. & Schröter, W. Combined ankyrin and spectrin deficiency in hereditary spherocytosis. Ann. Hematol. 67, 89–93 (1993).
3. Savvides, P., Shalev, O., John, K.M. & Lux, S.E. Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis. Blood 82, 2953–2960 (1993).
4. Lux, S.E., John, K.M. & Bennett, V. Analysis of cDNA for human erythrocyte ankyrin indicates a repeated structure with homology to tissue-differentiation and cell-cycle control proteins. Nature 344, 36–43 (1990).
5. Lux, S.E., John, K.M., Kopito, R.R. & Lodish, H.F. Cloning and characterization of band 3, the human erythrocyte anion-exchange protein (AE1). Proc. Natl. Acad. Sci. USA 86, 9088–9093 (1989).
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