Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s11033-011-1082-x.pdf
Reference58 articles.
1. Morton NE, MacKinney AA, Kosower N (1962) Genetics of spherocytosis. Am J Hum Genet 14:170–178
2. Godal HC, Heisto H (1981) High prevalence of increased osmotic fragility of red blood cells among Norwegian blood donors. Scand J Haematol 27:30–34
3. Tse WT, Lux SE (1999) Red blood cell membrane disorders. Br J Haematol 104:2–13
4. Eber SW, Pekrun A, Neufeldt A, Schroter W (1992) Prevalence of increased osmotic fragility of erythrocytes in German blood donors: screening using a modified glycerol lysis test. Ann Hematol 64:88–92
5. Delaunay J (2007) The molecular basis of hereditary red cell membrane disorders. Blood Rev 21:1–20
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