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

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

Research output: Contribution to journalArticle

3 Citations (Scopus)
Original languageEnglish
Pages (from-to)83-84
Number of pages2
JournalEuropean Journal of Pediatrics
Volume158
Issue number1
DOIs
Publication statusPublished - 1999

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Maternal phenylketonuria in two Sicilian families identified by maternal blood phenylalanine level screening and identification of a new phenylalanine hydroxylase gene mutation (P407L) [2]. / Corsello, G.; Bosco, P.; Call, F.; Greco, D.; Cammarata, M.; Ciaccio, M.; Piccione, M.; Romano, V.

In: European Journal of Pediatrics, Vol. 158, No. 1, 1999, p. 83-84.

Research output: Contribution to journalArticle

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AU - Piccione, M.

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