In the July 2011 issue of Movement Disorders, in the correspondence ‘‘Deletion in the Tyrosine Hydroxylase Genein a Patient with a Mild Phenotype’’ (volume 26, Issue 8, Pages 1558–1560), by Ormazabal et al., the affiliationswere listed incorrectly, the correct affiliations are listed below:

Aida Ormazabal, PhD,1,2* Mercedes Serrano, MD, PhD,1,2* Pedro Castro de Castro, MD,3 Estıbaliz Barredo-Val-derrama, MD,3 Judith Armstrong, PhD,2,4 Angels Garcia-Cazorla, MD, PhD,1,2 Jaume Campistol, MD, PhD,1,2

Claudio Toma, PhD,2,5 Bru Cormand, PhD,2,5 and Rafael Artuch, MD, PhD1,2

1Neuropediatric and Clinical Biochemistry Departments, Hospital Sant Joan de Deu, Barcelona, Spain, 2Centre forBiomedical Research on Rare Diseases (CIBER-ER), Instituto de Salud Carlos III, Barcelona, Spain, 3Neuropediat-ric Department, Hospital Gregorio Maranon, Madrid, Spain, 4Molecular Genetics Department, Hospital Sant Joande Deu, Barcelona, Spain, 5Department of Genetics, Faculty of Biology, University of Barcelona, and Institute ofBiomedicine of the University of Barcelona (IBUB), Spain

The publisher regrets the error.

------------------------------------------------------------Published online in Wiley Online Library (wileyonlinelibrary.com).DOI: 10.1002/mds.23946

E R R A T U M

2148 Movement Disorders, Vol. 26, No. 11, 2011