Clinical and Biochemical Characterization of Patients with Early Infantile Onset of Autosomal Recessive GTP Cyclohydrolase I Deficiency without Hyperphenylalaninemia

T. Opladen, G. Hoffmann, F. Horster, A.B. Hinz, K. Neidhardt, C. Klein, N. Wolf

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)157-161
JournalMovement Disorders
Issue number1
Publication statusPublished - 2011

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