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The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screening |
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Title: |
The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screening |
Author: |
Georgiou, Theodoros Ho, Gladys Vogazianos, Marios Dionysiou, Maria Nicolaou, Alexia Chappa, Georgia Nicolaides, Paola Stylianidou, Goula Christodoulou, John Drousiotou, Anthi |
Appeared in: |
Clinical biochemistry |
Paging: |
Volume 45 (2012) nr. 7-8 pages 5 p. |
Year: |
2012 |
Contents: |
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Publisher: |
The Canadian Society of Clinical Chemists |
Source file: |
Elektronische Wetenschappelijke Tijdschriften |
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