Phenylketonuria genotypes correlated to metabolic phenotype groups in Norway

European Journal of Pediatrics

Volumn 155, Issue 7, 1996, Pages 554-560

  Eiken, H G ^a   Knappskog, P M ^a   Motzfeldt, K ^b   Boman, H ^a   Apold, J ^a  

^a HAUKELAND UNIVERSITY HOSPITAL   (Norway)

^b UNIVERSITY OF OSLO   (Norway)

Author keywords

Metabolic phenotype; Phenylketonuria Genotype

Indexed keywords

PHENYLALANINE; PHENYLALANINE 4 MONOOXYGENASE;

ARTICLE; CHILD; CLINICAL FEATURE; DENATURING GRADIENT GEL ELECTROPHORESIS; DNA SEQUENCE; FEMALE; GENE MUTATION; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MALE; NORWAY; PHENOTYPE; PHENYLKETONURIA; PRIORITY JOURNAL; RESTRICTION MAPPING; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0029679603     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF01957904     Document Type: Article

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