Journal article

The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screening

Theodoros Georgiou, Gladys Ho, Marios Vogazianos, Maria Dionysiou, Alexia Nicolaou, Georgia Chappa, Paola Nicolaides, Goula Stylianidou, John Christodoulou, Anthi Drousiotou

Clinical Biochemistry | PERGAMON-ELSEVIER SCIENCE LTD | Published : 2012