Type 2 Hyperprolinemia: Absence of Δ 1 -Pyrroline-5-Carboxylic Acid Dehydrogenase Activity
Author:
Affiliation:
1. Metabolism Branch, National Cancer Institute, Bethesda, Maryland 20014
2. Department of Pediatrics, University of Colorado Medical Center, 4200 East Ninth Avenue, Denver 80220
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference11 articles.
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2. EFRON, M.L., FAMILIAL HYPERPROLINEMIA - REPORT OF A 2ND CASE ASSOCIATED WITH CONGENITAL RENAL MALFORMATIONS HEREDITARY HEMATURIA AND MILD MENTAL RETARDATION WITH DEMONSTRATION OF AN ENZYME DEFECT, NEW ENGLAND JOURNAL OF MEDICINE 272: 1243 (1965).
3. Goodman, S. I., Biochemical Medicine 10: 329 (1974).
4. Johnson, A. B., Journal of Biological Chemistry 237: 1876 (1962).
5. PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT
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