Detection of Inborn Errors of Metabolism: Galactosemia
Author:
Affiliation:
1. Department of Biophysics and Genetics, University of Colorado Medical Center, Denver 80220
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference20 articles.
1. BAKER, L, GALACTOSEMIA - SYMPTOMATIC AND ASYMPTOMATIC HOMOZYGOTES IN 1 NEGRO SIBSHIP, JOURNAL OF PEDIATRICS 68: 551 (1966).
2. BERGREN, W.R., GALACTONIC ACID IN GALACTOSEMIA - IDENTIFICATION IN URINE, SCIENCE 176: 683 (1972).
3. "Galactose Dehydrogenase," "Nothing Dehydrogenase," and Alcohol Dehydrogenase: Interrelation
4. CUATRECASAS, P, MAMMALIAN GALACTOSE DEHYDROGENASE .I. IDENTIFICATION AND PURIFICATION IN RAT LIVER, JOURNAL OF BIOLOGICAL CHEMISTRY 241: 5904 (1966).
5. CUATRECASAS, P, MAMMALIAN GALACTOSE DEHYDROGENASE .2. PROPERTIES SUBSTRATE SPECIFICITY AND DEVELOPMENTAL CHANGES, JOURNAL OF BIOLOGICAL CHEMISTRY 241: 5910 (1966).
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