The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screening Journal Articles Refereed uri icon

Overview

Authors

  • Authorship

    • GEORGIOU T
    • DROUSIOTOU A
    • HO G
    • VOGAZIANOS M
    • DIONYSIOU M
    • NICOLAOU A
    • CHAPPA G
    • NICOLAIDES P
    • STYLIANIDOU G
    • PROF John Christodoulou

Published in

  • Clinical Biochemistry

Time

Date/time value

  • 2012

Identity

Digital Object Identifier (DOI)

  • 10.1016/j.clinbiochem.2012.01.026

Additional Document Info

Parent Title

  • CLINICAL BIOCHEMISTRY

Volume

  • 45

Issue

  • 7-8

Publisher

  • Pergamon-Elsevier Science