1751-0473-9-4 1751-0473 Correction <p>Correction: Dispelling myths about rare disease registry system development</p> BellgardMatthewmbellgard@ccg.murdoch.edu.au BeroudChristophechristophe.beroud@inserm.fr ParkinsonKaykay.parkinson@alstrom.org.uk HarrisTesstess.harris@pkdcharity.org.uk AymeSegolenesegolene.ayme@inserm.fr BaynamGarethGareth.Baynam@health.wa.gov.au WeeramanthriTarunTarun.Weeramanthri@health.wa.gov.au DawkinsHughHugh.Dawkins@health.wa.gov.au HunterAdamahunter@ccg.murdoch.edu.au

Centre for Comparative Genomics, Murdoch University, Perth 6150, Western Australia

Faculté de Médecine de la Timone, INSERM UMR 910, Aix-Marseille Université, Marseille, France

AP-HM, Département de Génétique Médicale, Hôpital d’enfants Timone, Marseille, France

Alstrom Syndrome, 49 Southfield Ave, Paignton S, Devon TQ3 1LH, UK

Polycystic Kidney Disease Charity (UK), PKD International, Ciliopathy Alliance, London, UK

INSERM US14, ORPHANET 96 rue Didot, Paris 75014, France

Genetic Services of Western Australia, King Edward Memorial Hospital, Perth, Western Australia

School of Paediatrics and Child Health, University of Western Australia, Perth, Western Australia

Institute for Immunology and Infectious Diseases, Murdoch University, Perth, Western Australia

Office of Population Health Genomics, Public Health and Clinical Services Division, Department of Health, Government of Western Australia, Perth, Western Australia

School of Pathology & Laboratory Medicine, University of Western Australia, Perth, Western Australia

Curtin Health Innovation Research Institute, Curtin University of Technology, Perth, Western Australia

 Source Code for Biology and Medicine 1751-0473 2014 9 1 4 http://www.scfbm.org/content/9/1/4 2448496910.1186/1751-0473-9-4 171201428120143112014 2014Bellgard 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.

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.

 <p>Dispelling myths about rare disease registry system development</p>BellgardMBeroudCParkinsonKHarrisTAymeSBaynamGWeeramanthriTDawkinsHHunterASource Code Biol Med201382110.1186/1751-0473-8-2124131574