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Volumn 96, Issue 5, 1999, Pages 1811-1813
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Phenylketonuria: Old disease, new approach to treatment
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Author keywords
[No Author keywords available]
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Indexed keywords
PHENYLALANINE;
PHENYLALANINE 4 MONOOXYGENASE;
PHENYLALANINE AMMONIA LYASE;
AMINO ACID BLOOD LEVEL;
BIRTH DEFECT;
DOSE RESPONSE;
DRUG BIOAVAILABILITY;
DRUG EFFICACY;
DRUG MECHANISM;
ENZYME REPLACEMENT;
GENETIC ASSOCIATION;
HUMAN;
INTRAPERITONEAL DRUG ADMINISTRATION;
MENTAL DEFICIENCY;
NONHUMAN;
NOTE;
ORAL DRUG ADMINISTRATION;
PATHOGENESIS;
PATIENT COMPLIANCE;
PHENYLKETONURIA;
PRIORITY JOURNAL;
PROTEIN RESTRICTION;
TREATMENT INDICATION;
TREATMENT OUTCOME;
ANIMALS;
DIET;
HUMANS;
MICE;
MICE, MUTANT STRAINS;
PHENYLALANINE;
PHENYLALANINE AMMONIA-LYASE;
PHENYLKETONURIAS;
RECOMBINANT PROTEINS;
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EID: 0033514946
PISSN: 00278424
EISSN: None
Source Type: Journal
DOI: 10.1073/pnas.96.5.1811 Document Type: Note |
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Times cited : (57)
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References (42)
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