Author:
Kahn A.,Kaplan J. C.,Dreyfus J. C.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference159 articles.
1. Alagille, D., Fleury, J., Odièvre, M.: Déficit congénital en 2,3-diphosphoglycerate mutase. Soc. Med. Hôp. Paris 115, 493?499 (1964)
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. Blood 41, 691?699 (1973a)
3. Arnold, H., Engelhardt, R., Löhr, G. W., Jacobi, H., Liebold, I.: Glucosephosphat-Isomerase Typ Recklinghausen: Eine neue Defektvariante mit hämolytischer Anämie. Klin. Wochenschr. 51, 1198?1204 (1973b)
4. Arnold, H., Hoffmann, A., Blume, K. G., Engelhardt, R., Löhr, G. W.: Zur Frage gewebespezifischer Isoenzyme der Glucosephosphatisomerase des Menschen. Klin. Wochenschr. 52, 149?151 (1974)
5. Baughan, M. A., Valentine, W. N., Paglia, D. E., Ways, P. O., Simon, E. R., Marsch, Q. B. de: Hereditary hemolytic anemia with glucose phosphate isomerase (GPI) deficiency, a new enzyme defect of human erythrocytes. Blood 32, 236?249 (1968)
Cited by
25 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