1750-1172-8-73 1750-1172 Correction <p>Correction: Disease and patient characteristics in NP-C patients: findings from an international disease registry</p> PattersonCMarcpatterson.marc@mayo.edu MengelEugenEugenMg@t-online.de WijburgAFritsf.a.wijburg@amc.uva.nl MullerAudreyaudrey.muller@actelion.com SchwierinBarbarabarbara.schwierin@actelion.com DrevonHarirharir.drevon@numerus-ltd.com VanierTMarievaniermtv@gmail.com PinedaMercépineda@hsjdbcn.org

Mayo Clinic, Rochester, MN, USA

Villa Metabolica, ZKJM, MC, University of Mainz,, Mainz, Germany

Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands

Actelion Pharmaceuticals Ltd, Allschwil, Switzerland

Numerus Ltd, Wokingham, UK

INSERM Unit 820, Lyon, France

Fundació Hospital Sant Joan de Déu, Barcelona, Spain

Department of Neurology, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA

 Orphanet Journal of Rare Diseases 1750-1172 2013 8 1 73 http://www.ojrd.com/content/8/1/73 10.1186/1750-1172-8-73 7520137520131452013 2013Patterson et al.; licensee BioMed Central Ltd.This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Correction

After the publication of this work 1 it was brought to the authors attention that Figure 1 contained an inversion in the color of the triangles, where yellow which should be "diagnosis" is said to be "first miglustat use", and blue which should be " first miglustat use" is said to be " diagnosis". The correct figure is given below:

<p>Figure 1</p>

Overview of patient and disease characteristics

Overview of patient and disease characteristics. We regret any inconvenience that this inaccuracy may have caused.

 <p>Disease and patient characteristics in NP-C patients: findings from an international disease registry</p>PattersonMCEugenMWijburgFAAudreyMBarbaraSHarirDVanierMTMercéPOrphanet Journal of Rare Diseases201381210.1186/1750-1172-8-12355839923324478