Open Access

Erratum to: Disease and patient characteristics in NP-C patients: findings from an international disease registry

  • Marc C Patterson1, 8Email author,
  • Eugen Mengel2,
  • Frits A Wijburg3,
  • Audrey Muller4,
  • Barbara Schwierin4,
  • Harir Drevon5,
  • Marie T Vanier6 and
  • Mercé Pineda7
Orphanet Journal of Rare Diseases20138:73

https://doi.org/10.1186/1750-1172-8-73

Received: 7 May 2013

Accepted: 7 May 2013

Published: 14 May 2013

The original article was published in Orphanet Journal of Rare Diseases 2013 8:12

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:
Figure 1

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

Notes

Declarations

Authors’ Affiliations

(1)
Mayo Clinic
(2)
Villa Metabolica, ZKJM, MC, University of Mainz
(3)
Academic Medical Centre, University of Amsterdam
(4)
Actelion Pharmaceuticals Ltd
(5)
Numerus Ltd
(6)
INSERM Unit 820
(7)
Fundació Hospital Sant Joan de Déu
(8)
Department of Neurology, Mayo Clinic

References

  1. Patterson MC, Eugen M, Wijburg FA, Audrey M, Barbara S, Harir D, Vanier MT, Mercé P: Disease and patient characteristics in NP-C patients: findings from an international disease registry. Orphanet Journal of Rare Diseases. 2013, 8: 12-10.1186/1750-1172-8-12.PubMed CentralPubMedView ArticleGoogle Scholar

Copyright

© Patterson et al.; licensee BioMed Central Ltd. 2013

This article is published under license to 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.

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