Galactokinase deficiency in a newborn infant.
Open Access
- 1 December 1971
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 46 (250) , 864-866
- https://doi.org/10.1136/adc.46.250.864
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- A PATIENT WITH HEREDITARY GALACTOKINASE DEFICIENCYActa Paediatrica, 1970
- [Partial and transitory erythrocyte galactokinase deficiency in a newborn. Biochemical study].1970
- Das Fehlen von Insulinstimulation durch Galactose bei Patienten mit Galactokinase-MangelDiabetologia, 1969
- HYPERGALACTOSEMIA AND GALACTOSURIA DUE TO GALACTOKINASE DEFICIENCY IN A NEWBORNPediatrics, 1968
- Hereditary Galactokinase Deficiency, a Newly Recognized Cause of Juvenile Cataracts31Pediatric Research, 1966
- DEFICIENCY OF ERYTHROCYTE GALACTOKINASE IN A PATIENT WITH GALACTOSE DIABETESThe Lancet, 1965
- Formation of Polyols by the Lens of the Rat with ‘Sugar’ CataractNature, 1959