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
Th. Georgiou was supported by the Cyprus Human Resources Authority through a training grant.