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Erratum to: Dispelling myths about rare disease registry system development

  • The original article was published in Source Code for Biology and Medicine 2013 8:21

Correction

After publication of this work [1], we noted that we inadvertently failed to include important Acknowledgments in our final version of the manuscript. Please see below the modification:

Acknowledgements

The authors received funding from the Australian National Health and Medical Research Council (APP1055319) and EU FP7 Project (HEALTH.2012.2.1.1-1-C): RD Connect: An integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research. The authors wish to acknowledge their involvement in the International Rare Disease Research Consortium.

References

  1. 1.

    Bellgard M, Beroud C, Parkinson K, Harris T, Ayme S, Baynam G, Weeramanthri T, Dawkins H, Hunter A: Dispelling myths about rare disease registry system development. Source Code Biol Med. 2013, 8: 21-10.1186/1751-0473-8-21.

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Author information

Correspondence to Matthew Bellgard.

Additional information

The online version of the original article can be found at 10.1186/1751-0473-8-21

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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 credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Bellgard, M., Beroud, C., Parkinson, K. et al. Erratum to: Dispelling myths about rare disease registry system development. Source Code Biol Med 9, 4 (2014). https://doi.org/10.1186/1751-0473-9-4

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