Galactose-1-phosphate uridyl transferase deficiency due to Duarte/galactosemia combined variation: Clinical and biochemical studies
- 1 March 1978
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 92 (3) , 390-393
- https://doi.org/10.1016/s0022-3476(78)80425-9
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
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- Newborn Screening for Metabolic DisordersNew England Journal of Medicine, 1973
- Galactosemia Screening of Newborns in MassachusettsNew England Journal of Medicine, 1971
- Unstable galactose-1-phosphate uridyl transferase: A new variant of galactosemiaThe Journal of Pediatrics, 1971
- An improved electrophoretic procedure for galactose-l-phosphate uridyl transferase: Demonstration of multiple activity bands with the duarte variantBiochemical and Biophysical Research Communications, 1969
- Electrophoretic abnormality of galactose-1-phosphate uridyl transferase in galactosemiaBiochemical and Biophysical Research Communications, 1969
- GalactosemiaBiochemical Medicine, 1967
- Improved method for measuring galactose-1-phosphate uridyl transferase activity of erythrocytesClinica Chimica Acta; International Journal of Clinical Chemistry, 1966