The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screening
| Autor: | Georgiou, Theodoros a, Ho, Gladys b, Vogazianos, Marios c, Dionysiou, Maria a, Nicolaou, Alexia c, Chappa, Georgia d, Nicolaides, Paola e, Stylianidou, Goula d, 1, Christodoulou, John b, f, Drousiotou, Anthi a, ⁎ |
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| Zdroj: | In Clinical Biochemistry May 2012 45(7-8):588-592 |
| Databáze: | ScienceDirect |
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