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
Volume26
Issue number1
DOIs
Publication statusPublished - 2011

Cite this

@article{7b3b59d49adc4bdcb3440dcec4feaf9c,
title = "Clinical and Biochemical Characterization of Patients with Early Infantile Onset of Autosomal Recessive GTP Cyclohydrolase I Deficiency without Hyperphenylalaninemia",
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",
language = "Undefined/Unknown",
volume = "26",
pages = "157--161",
journal = "Movement Disorders",
issn = "0885-3185",
publisher = "John Wiley and Sons Inc.",
number = "1",

}

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 journalArticleAcademicpeer-review

TY - JOUR

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

AU - Opladen, T.

AU - Hoffmann, G.

AU - Horster, F.

AU - Hinz, A.B.

AU - Neidhardt, K.

AU - Klein, C.

AU - Wolf, N.

PY - 2011

Y1 - 2011

U2 - 10.1002/mds.23329

DO - 10.1002/mds.23329

M3 - Article

VL - 26

SP - 157

EP - 161

JO - Movement Disorders

JF - Movement Disorders

SN - 0885-3185

IS - 1

ER -