Maternal phenylketonuria in two Sicilian families identified by maternal blood phenylalanine level screening and identification of a new phenylalanine hydroxylase gene mutation (P407L) [2]

European Journal of Pediatrics

Volumn 158, Issue 1, 1999, Pages 83-84

  Corsello, G ^a   Bosco, P ^a   Call, F ^a   Greco, D ^a   Cammarata, M ^a   Ciaccio, M ^a   Piccione, M ^a   Romano, V ^a  

^a OASI RESEARCH INSTITUTE IRCCS   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE; PHENYLALANINE 4 MONOOXYGENASE;

GENE MUTATION; HETEROZYGOTE; HUMAN; HYPERPHENYLALANINEMIA; ITALY; LETTER; NEWBORN SCREENING; PEDIGREE ANALYSIS; PHENYLKETONURIA; PRIORITY JOURNAL;

FEMALE; GENETIC SCREENING; HUMANS; INFANT, NEWBORN; ITALY; MUTATION; NEONATAL SCREENING; PEDIGREE; PHENYLALANINE; PHENYLALANINE HYDROXYLASE; PHENYLKETONURIA, MATERNAL; PHENYLKETONURIAS; PREGNANCY;

EID: 0033063945     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004310051018     Document Type: Letter

References (4)