Galactokinase deficiency: Clinical and biochemical findings in a new kindred
- 31 July 1972
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 81 (1), 50-55
- https://doi.org/10.1016/s0022-3476(72)80373-1
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
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- Cyclic Adenosine Monophosphate in BacteriaScience, 1970
- Infantile Metachromatic LeukodystrophyNew England Journal of Medicine, 1970
- Galactose-1-phosphate uridyltransferase and galactokinase activity in cultured human diploid fibroblasts and peripheral blood leukocytesJCI Insight, 1969
- Human Hepatic Uridine Diphosphate Galactose PyrophosphorylasePublished by Elsevier ,1969
- Hereditary Galactokinase Deficiency, a Newly Recognized Cause of Juvenile Cataracts31Pediatric Research, 1966
- Skin Biopsy for Cell CultureNature, 1963
- Galactose metabolism and galactosemiaAmerican Journal Of Medicine, 1959
- Galactosemia, a congenital defect in a nucleotide transferaseBiochimica et Biophysica Acta, 1956