Correction: Dispelling myths about rare disease registry system development.

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Correction: Dispelling myths about rare disease registry

system development.

Matthew Bellgard, Christophe Béroud, Kay Parkinson, Tess Harris, Segolene

Ayme, Gareth Baynam, Tarun Weeramanthri, Hugh Dawkins, Adam Hunter

To cite this version:

Matthew Bellgard, Christophe Béroud, Kay Parkinson, Tess Harris, Segolene Ayme, et al.. Correction:

Dispelling myths about rare disease registry system development.. Source Code for Biology and

Medicine, BioMed Central, 2014, 9 (1), pp.4. �10.1186/1751-0473-9-4�. �inserm-00943519�

C O R R E C T I O N

Open Access

Correction: Dispelling myths about rare disease

registry system development

Matthew Bellgard

, Christophe Beroud

, Kay Parkinson

, Tess Harris

, Segolene Ayme

, Gareth Baynam

,

Tarun Weeramanthri

, Hugh Dawkins

and Adam Hunter

Correction

After publication of this work [1], we noted that we

in-advertently failed to include important

Acknowledg-ments 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

re-search. The authors wish to acknowledge their involvement

in the International Rare Disease Research Consortium.

Author details

1_{Centre for Comparative Genomics, Murdoch University, Perth 6150, Western}

Australia.2_{Faculté de Médecine de la Timone, INSERM UMR 910, Aix-Marseille}

Université, Marseille, France.3_{AP-HM, Département de Génétique Médicale,}

Hôpital d’enfants Timone, Marseille, France.4_{Alstrom Syndrome, 49}

Southfield Ave, Paignton S, Devon TQ3 1LH, UK.5_{Polycystic Kidney Disease}

Charity (UK), PKD International, Ciliopathy Alliance, London, UK.6_INSERM

US14, ORPHANET 96 rue Didot, Paris 75014, France.7_{Genetic Services of}

Western Australia, King Edward Memorial Hospital, Perth, Western Australia.

8_{School of Paediatrics and Child Health, University of Western Australia,}

Perth, Western Australia.9_{Institute for Immunology and Infectious Diseases,}

Murdoch University, Perth, Western Australia.10_{Office of Population Health}

Genomics, Public Health and Clinical Services Division, Department of Health, Government of Western Australia, Perth, Western Australia.11_{School of}

Pathology & Laboratory Medicine, University of Western Australia, Perth, Western Australia.12_{Curtin Health Innovation Research Institute, Curtin}

University of Technology, Perth, Western Australia.

Received: 17 January 2014 Accepted: 28 January 2014 Published: 31 January 2014

Reference

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.

doi:10.1186/1751-0473-9-4

Cite this article as: Bellgard et al.: Correction: Dispelling myths about rare disease registry system development. Source Code for Biology and Medicine 2014 9:4.

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* Correspondence:mbellgard@ccg.murdoch.edu.au

1_{Centre for Comparative Genomics, Murdoch University, Perth 6150, Western}

Australia

Full list of author information is available at the end of the article

© 2014 Bellgard 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 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.

Bellgard et al. Source Code for Biology and Medicine 2014, 9:4 http://www.scfbm.org/content/9/1/4