Defect in glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia type II (HEMPAS)
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1984.tb01271.x/fullpdf
Reference35 articles.
1. Congenital Dyserythropoietic Anaemia, Types I and II: Aberrant Pattern of Erythrocyte Membrane Proteins in CDA II, as Revealed by Two-dimensional Polyacrylamide Gel Electrophoresis
2. Red cell membrane protein anomalies in congenital dyserythropoietic anaemia, type II (HEMPAS)
3. The monosaccharide transport system of the human erythrocyte. Orientation upon reconstitution
4. “Western Blotting”: Electrophoretic transfer of proteins from sodium dodecyl sulfate-polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein A
5. Blood-group-I activity associated with band 3, the major intrinsic membrane protein of human erythrocytes
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5. Congenital dyserythropoietic anemia type II (CDAII/HEMPAS): Where are we now?;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2009-09
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