Hexokinase Deficiency in Erythrocytes: A New Variant in 5 Members of a Finnish Family
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1979.tb02799.x/fullpdf
Reference14 articles.
1. Normal and variant isoenzymes of human blood cell hexokinase and the isoenzyme patterns in hemolytic anemia;Altay;Blood,1970
2. Congenital nonspherocytic hemolytic anemia with an unstable hexokinase variant;Board;Blood,1978
3. Erythrocyte metabolism and function: Hexokinase inhibition by 2,3-diphos-phoglycerate and interaction with ATP and Mg2+;Brewer;Biochim Biophys Acta,1969
4. Oxygen-hemoglobin dissociation curves: Effect of inherited enzyme defects of the red cells;Delivoria-Papadopoulos;Science,1969
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Hexokinase: gene structure and mutations;Best Practice & Research Clinical Haematology;2000-03
2. A new metabolic muscle disease due to abnormal hexokinase activity.;Journal of Neurology, Neurosurgery & Psychiatry;1988-02-01
3. Human erythrocyte hexokinase deficiency: a new variant with abnormal kinetic properties;British Journal of Haematology;1985-09
4. Hexokinase “New Hyde Park”: A low activity erythrocyte isozyme in a chinese kindred;American Journal of Hematology;1981-04
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