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

✍ Scribed by G. Corsello; P. Bosco; F. Calì; D. Greco; M. Cammarata; M. Ciaccio; M. Piccione; V. Romano

• Publisher: Springer
• Year: 1999
• Tongue: English
• Weight: 84 KB
• Volume: 158
• Category: Article
• ISSN: 0340-6997
• DOI: 10.1007/s004310051018