Author:
Kahn A.,North M. L.,Cottreau D.,Giron G.,Lang J. M.,Oberling F.
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference18 articles.
1. Beutler, E., Yoshida, A.: Human glucose-6-phosphate dehydrogenase variants: A supplementary tabulation. Ann. Hum. Genet. 37, 151?155 (1973)
2. Goetz, O., Müller-Elbracht, H. J.: Paroxysmal nocturnal hemoglobinuria: Role of the C3 activator system. New Engl. J. Med. 286, 180?184 (1972)
3. Kahn, A., Cottreau, D., Boivin, P.: Molecular mechanism of glucose-6-phosphate dehydrogenase deficiency. Humangenetik 25, 101?109 (1974)
4. Kahn, A., Hakim, J., Cottreau, D., Boivin, P.: Gd(-) Matam, an african G6PD variant with enzyme deficiency. Biochemical and immunological properties in various hemopoitic tissues. Clin. Chim. Acta 59, 183?190 (1975)
5. Kahn, A., Esters, A., Habedank, M.: Gd(-) Aachen, a new variant of deficient glucose-6-phosphate dehydrogenase. Clinical genetic and biological aspects. Hum. Genet. 32, 171?180 (1976a)
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