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

doi:10.1002/mds.23329

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

Pediatrics

Research output: Contribution to journal › Article › Academic › peer-review

Original language	Undefined/Unknown
Pages (from-to)	157-161
Journal	Movement Disorders
Volume	26
Issue number	1
DOIs	https://doi.org/10.1002/mds.23329
Publication status	Published - 2011

Access to Document

10.1002/mds.23329

Cite this

Opladen, T., Hoffmann, G., Horster, F., Hinz, A. B., Neidhardt, K., Klein, C., & Wolf, N. (2011). Clinical and Biochemical Characterization of Patients with Early Infantile Onset of Autosomal Recessive GTP Cyclohydrolase I Deficiency without Hyperphenylalaninemia. Movement Disorders, 26(1), 157-161. https://doi.org/10.1002/mds.23329

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

year = "2011",

doi = "10.1002/mds.23329",

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journal = "Movement Disorders",

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Clinical and Biochemical Characterization of Patients with Early Infantile Onset of Autosomal Recessive GTP Cyclohydrolase I Deficiency without Hyperphenylalaninemia. / Opladen, T.; Hoffmann, G.; Horster, F.; Hinz, A.B.; Neidhardt, K.; Klein, C.; Wolf, N.

In: Movement Disorders, Vol. 26, No. 1, 2011, p. 157-161.

Research output: Contribution to journal › Article › Academic › peer-review

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T1 - Clinical and Biochemical Characterization of Patients with Early Infantile Onset of Autosomal Recessive GTP Cyclohydrolase I Deficiency without Hyperphenylalaninemia

AU - Opladen, T.

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AU - Horster, F.

AU - Hinz, A.B.

AU - Neidhardt, K.

AU - Klein, C.

AU - Wolf, N.

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