Clinical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia

T Opladen, GF Hoffmann, F Hörster, AB Hinz, K Neidhardt, C Klein, NI Wolf
  • Neuropediatrics, March 2011, Thieme Publishing Group
  • DOI: 10.1055/s-0031-1273970
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The following have contributed to this page: Dr Nicole I Wolf