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

Pubmed ID: 
22330942
Year: 
2012
Month: 
May
Volume: 
45
Issue: 
7-8
Citation: 
Georgiou T, Ho G, Vogazianos M, Dionysiou M, Nicolaou A, Chappa G, Nicolaides P, Stylianidou G, Christodoulou J, Drousiotou A. The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screening. CLINICAL BIOCHEMISTRY 45 (7-8) : 588 - 92(2012) PubMed