Isoelectrofocusing of erythrocyte galactose 1 phospho uridyl transferase in a family with both galactosemia and duarte variants |
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| Authors: | F. Schapira C. Gregori J. Banroques M. Vidailhet S. Despoisses C. Vigneron |
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| Affiliation: | (1) Institut de Pathologie Moléculaire, 24, rue du Faubourg St-Jacques, F-75014 Paris, France;(2) Service de Médecine Infantile A, Centre Hospitalier Régional de Nancy, 29, Avenue du Maréchal de Lattre de Tassigny, F-54037 Nancy Cedex, France;(3) Laboratoire de Chimie hématologique, Centre Régional de Transfusion Sanguine, 9-11, rue Lionnois, F-54500 Vandoeuvre, France |
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| Abstract: | Summary A family with the presence of the genes for both galactosemia and the Duarte variant is described. Galactose 1 phospho uridyl transferase has been studied not only by electrophoresis on starch gel, but also by isoelectrofocusing on thin-layer acrylamide.Normal and variant transferases were resolved into three bands, the isoelectric point of which was between 5.40 and 5.10 for the normal subjects, and between 5.25 and 4.95 for subjects with the Duarte variant. |
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