The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screening.
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P. Nicolaides | A. Drousiotou | J. Christodoulou | G. Ho | T. Georgiou | G. Stylianidou | G. Chappa | M. Vogazianos | Maria Dionysiou | A. Nicolaou