Potential conflict of interest: Nothing to report.
Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia†
Version of Record online: 3 SEP 2010
Copyright © 2010 Movement Disorder Society
Volume 26, Issue 1, pages 157–161, January 2011
How to Cite
Opladen, T., Hoffmann, G., Hörster, F., Hinz, A.-B., Neidhardt, K., Klein, C. and Wolf, N. (2011), Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia. Mov. Disord., 26: 157–161. doi: 10.1002/mds.23329
- Issue online: 14 FEB 2011
- Version of Record online: 3 SEP 2010
- Manuscript Accepted: 2 JUN 2010
- Manuscript Revised: 18 FEB 2010
- Manuscript Received: 10 DEC 2009
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