Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia - Opladen, Thomas; Hoffmann, Georg F.; Hörster, Friederike; Hinz, Anne-Bärbel; Neidhardt, Katharina; Klein, Christine; Wolf, Nicole (Movement disorders, 2011)
First published online: 03 September 2010