Uridine diphosphate galactose 4-epimerase deficiency
- 1 February 1981
- journal article
- case report
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 135 (3) , 303-304
- https://doi.org/10.1007/bf00442108
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Galactose metabolism, hereditary defects and their clinical significancePublished by Springer Nature ,1980
- Assignment of a gene for uridine diphosphate galactose-4-epimerase to human chromosome 1 by somatic cell hybridization, with evidence for a regional assignment to 1pter→1p21Cytogenetic and Genome Research, 1979
- Uridine diphosphate galactose 4'-epimerase deficiency. IV. Report of eight cases in three families.1977
- Uridine diphosphate galactose 4-epimerase deficiency. II. Clinical follow-up, biochemical studies and family investigation.1973
- Deficiency of uridine diphosphate galactose 4-epimerase in blood cells of an apparently healthy infant. Preliminary communication.1972
- Hereditary Galactokinase Deficiency, a Newly Recognized Cause of Juvenile Cataracts31Pediatric Research, 1966
- DEFICIENCY OF ERYTHROCYTE GALACTOKINASE IN A PATIENT WITH GALACTOSE DIABETESThe Lancet, 1965