Detection of heterozygotes for galactokinase deficiency in a human population
- 1 November 1968
- journal article
- Published by Springer Nature in Biochemical Genetics
- Vol. 2 (3) , 219-230
- https://doi.org/10.1007/bf01474761
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Erythrocyte galactose-1-phosphate uridyl transferase and glucose-6-phosphate dehydrogenase activity in the population of the Rhondda FachClinica Chimica Acta; International Journal of Clinical Chemistry, 1967
- Frequency of Heterozygotes for Hereditary Galactosaemia in a Normal PopulationHuman Heredity, 1967
- Electrophoretic Variation of Galactose-1-Phosphate UridyltransferaseScience, 1966
- Galactitol excretion in the urine of a galactokinase-deficient manBiochemical and Biophysical Research Communications, 1966
- Galactose Metabolism and Cell "Sociology"Science, 1965
- DEFICIENCY OF ERYTHROCYTE GALACTOKINASE IN A PATIENT WITH GALACTOSE DIABETESThe Lancet, 1965
- Skin Biopsy for Cell CultureNature, 1963
- A study of the genetics of galactosaemiaAnnals of Human Genetics, 1962
- ENZYMIC EVIDENCE OF A GALACTOSEMIC TRAIT IN PARENTS OF GALACTOSEMIC CHILDREN*Annals of Human Genetics, 1958
- Congenital Galactosemia, a Single Enzymatic Block in Galactose MetabolismScience, 1956