Red cell membrane protein anomalies in congenital dyserythropoietic anaemia, type II (HEMPAS)
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1982.tb01956.x/fullpdf
Reference32 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. AN ERYTHROCYTE MEMBRANE-PROTEIN ANOMALY IN MARCH HÆMOGLOBINURIA
3. Association between ankyrin and the cytoplasmic domain of band 3 isolated from the human erythrocyte membrane.
4. [87] Fluorescence measurements
5. Peptide mapping by limited proteolysis in sodium dodecyl sulfate and analysis by gel electrophoresis.
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1. Whole-exome analysis to detect congenital hemolytic anemia mimicking congenital dyserythropoietic anemia;International Journal of Hematology;2018-06-23
2. Characteristic phenotypes associated with congenital dyserythropoietic anemia (type II) manifest at different stages of erythropoiesis;Haematologica;2013-08-09
3. Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach;Haematologica;2012-10-12
4. The COPII pathway and hematologic disease;Blood;2012-07-05
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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