The spectrum of mutations identified in Cypriot patients...

Clinical Biochemistry 2012 Vol. 45; Iss. 7-8

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
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Volume:
45
Year:
2012
Language:
english
DOI:
10.1016/j.clinbiochem.2012.01.026
File:
PDF, 333 KB
english, 2012
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