The primary molecular defects in phenylketonuria and its variants
Author:
Publisher
Elsevier BV
Subject
Biochemistry
Reference81 articles.
1. Phenylalaninemia;Auerbach,1967
2. Isozymes of phenylalanine hydroxylase;Barranger;Science,1972
3. A new molecular defect in phenylketonuria;Bartholome;Lancet,1974
4. l-DOPA and 5-hyd-roxytryptophan therapy in phenylketonuria with normal phenylalanine-hydroxylase activity;Bartholome;Lancet,1975
5. Immunological detection of phenylalanine hydroxylase in phenylketonuria;Bartholome;Lancet,1976
Cited by 19 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Aspartame Consumption in Normal Individuals and Carriers for Phenylketonuria;Dietary Phenylalanine and Brain Function;1988
2. A monoclonal antibody to the phosphorylated form of phenylalanine hydroxylase. Definition of the phosphopeptide epitope;Biochemical Journal;1987-06-15
3. The W and L allelic forms of phenylalanine hydroxylase in the rat differ by a threonine to isoleucine substitution;Biochemical Journal;1986-06-15
4. A novel two-dimensional polyacrylamide-gel pattern, which may be due to allelic genes, of phenylalanine hydroxylase in monkeys;Biochemical Journal;1985-10-01
5. BIOSYNTHESIS AND METABOLISM OF TETRAHYDROBIOPTERIN AND MOLYBDOPTERIN;Annual Review of Biochemistry;1985-06
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