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Volumn 280, Issue , 1980, Pages 1-80
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Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood.
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NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
DIAGNOSTIC AGENT;
PHENYLALANINE;
PHENYLALANINE 4 MONOOXYGENASE;
BLOOD;
CLASSIFICATION;
DISORDERS OF AMINO ACID AND PROTEIN METABOLISM;
GENETICS;
HETEROZYGOTE DETECTION;
HUMAN;
MENTAL DEFICIENCY;
NEWBORN;
NUTRITIONAL DEFICIENCY;
PHENOTYPE;
PHENYLKETONURIA;
REVIEW;
AMINO ACID METABOLISM, INBORN ERRORS;
HETEROZYGOTE DETECTION;
HUMAN;
INFANT, NEWBORN;
MENTAL RETARDATION;
PHENOTYPE;
PHENYLALANINE;
PHENYLALANINE HYDROXYLASE;
PHENYLKETONURIAS;
SUPPORT, NON-U.S. GOV'T;
TERMINOLOGY;
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EID: 0019288144
PISSN: 03008843
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
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Times cited : (119)
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References (230)
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