Maternal phenylketomuria in two Sicilian families identified by maternal blood phenylalanine level screening and identification of a new phenylalanine hydroxylase gene mutation (P407L)
G. Corsello et al., Maternal phenylketomuria in two Sicilian families identified by maternal blood phenylalanine level screening and identification of a new phenylalanine hydroxylase gene mutation (P407L), EUR J PED, 158(1), 1999, pp. 83-84