Congenital nonspherocytic hemolytic anemia associated with glucosephosphate isomerase deficiency: Variant Paderborn
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Genetics (clinical),Drug Discovery,Molecular Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF01488625.pdf
Reference26 articles.
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2. Arnold, H., Blume, K.G., Engelhardt, R., Löhr, G.W.: Glucose-phosphate isomerase deficiency: Evidence for in vivo instability of an enzyme variant with hemolysis. Blood41, 691?699 (1973)
3. Arnold, H., Blume, K.G., Löhr, G.W., Schröter, W., Koch, H.H., Wonneberger, B.: Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: A new variant (type Nordhorn). II. Purification and biochemical properties of the defective enzyme. Pediat. Res.8, 26?30 (1974)
4. Arnold, H., Seiberling, M., Blume, K.G., Löhr, G.W.: Immunological studies on glucosephosphate isomerase deficiency: Instability and impaired synthesis of the defective enzyme. Klin. Wschr.53, 1135?1136 (1975)
5. Barthelmai, W., Vetrella, M., Eschenbach, C., Jehn, E.: Leukocytenisolierungen aus kleinen Blutvolumina. Klin. Wschr,49, 263?268 (1971)
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3. Clinical symptoms and biochemical properties of three new glucosephosphate isomerase variants;Blut;1986-07
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5. The first stable variant of erythrocyte glucose-phosphate isomerase associated with severe hemolytic anemia;American Journal of Hematology;1980-08
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