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Volumn 101, Issue 12, 1998, Pages 2613-2614
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An ongoing debate over phenylalanine hydroxylase deficiency in phenylketonuria
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Author keywords
[No Author keywords available]
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Indexed keywords
PHENYLALANINE;
PHENYLALANINE 4 MONOOXYGENASE;
ALLELE;
CLINICAL ARTICLE;
CONTROLLED STUDY;
EDITORIAL;
ENZYME ACTIVITY;
ENZYME DEFICIENCY;
GENE MUTATION;
HUMAN;
HYDROXYLATION;
HYPERPHENYLALANINEMIA;
INBORN ERROR OF METABOLISM;
MENTAL DEFICIENCY;
MOLECULAR CLONING;
PHENYLKETONURIA;
PRIORITY JOURNAL;
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EID: 0032526242
PISSN: 00219738
EISSN: None
Source Type: Journal
DOI: 10.1172/JCI3928 Document Type: Editorial |
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Times cited : (8)
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References (11)
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