Aida Ormazabal and Mercedes Serrano contributed equally to this article. Relevant conflicts of interest/financial disclosures: Nothing to report. Full financial disclosures and author roles may be found in the online version of this article. Support was received from the Biomedical Network Research Centre on Rare Diseases (CIBER-ER, ISCIII), grant FIS PS09/01132, and Agència de Gestió d'Ajuts Universitaris i de Recerca—AGAUR (2009-SGR-00971). Dr. Toma and Dr. Serrano were supported by a CIBER-ER contract and Dr. Artuch by ISCIII (intensificación de la actividad investigadora).
Letter to the Editor
Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype†
Version of Record online: 4 APR 2011
Copyright © 2010 Movement Disorder Society
Volume 26, Issue 8, pages 1558–1560, July 2011
How to Cite
Ormazabal, A., Serrano, M., Garcia-Cazorla, A., Campistol, J., Artuch, R., Castro de Castro, P., Barredo-Valderrama, E., Armstrong, J., Toma, C. and Cormand, B. (2011), Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype. Mov. Disord., 26: 1558–1560. doi: 10.1002/mds.23564
- Issue online: 21 JUL 2011
- Version of Record online: 4 APR 2011
- Manuscript Accepted: 10 NOV 2010
- Manuscript Revised: 1 NOV 2010
- Manuscript Received: 2 SEP 2010
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