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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Correction: Dispelling myths about rare disease registry system development</title><author><name sortKey="Bellgard, Matthew" sort="Bellgard, Matthew" uniqKey="Bellgard M" first="Matthew" last="Bellgard">Matthew Bellgard</name><affiliation><nlm:aff id="I1">Centre for Comparative Genomics, Murdoch University, Perth 6150, Western Australia</nlm:aff></affiliation></author><author><name sortKey="Beroud, Christophe" sort="Beroud, Christophe" uniqKey="Beroud C" first="Christophe" last="Beroud">Christophe Beroud</name><affiliation><nlm:aff id="I2">Faculté de Médecine de la Timone, INSERM UMR 910, Aix-Marseille Université, Marseille, France</nlm:aff></affiliation><affiliation><nlm:aff id="I3">AP-HM, Département de Génétique Médicale, Hôpital d’enfants Timone, Marseille, France</nlm:aff></affiliation></author><author><name sortKey="Parkinson, Kay" sort="Parkinson, Kay" uniqKey="Parkinson K" first="Kay" last="Parkinson">Kay Parkinson</name><affiliation><nlm:aff id="I4">Alstrom Syndrome, 49 Southfield Ave, Paignton S, Devon TQ3 1LH, UK</nlm:aff></affiliation></author><author><name sortKey="Harris, Tess" sort="Harris, Tess" uniqKey="Harris T" first="Tess" last="Harris">Tess Harris</name><affiliation><nlm:aff id="I5">Polycystic Kidney Disease Charity (UK), PKD International, Ciliopathy Alliance, London, UK</nlm:aff></affiliation></author><author><name sortKey="Ayme, Segolene" sort="Ayme, Segolene" uniqKey="Ayme S" first="Segolene" last="Ayme">Segolene Ayme</name><affiliation><nlm:aff id="I6">INSERM US14, ORPHANET 96 rue Didot, Paris 75014, France</nlm:aff></affiliation></author><author><name sortKey="Baynam, Gareth" sort="Baynam, Gareth" uniqKey="Baynam G" first="Gareth" last="Baynam">Gareth Baynam</name><affiliation><nlm:aff id="I7">Genetic Services of Western Australia, King Edward Memorial Hospital, Perth, Western Australia</nlm:aff></affiliation><affiliation><nlm:aff id="I8">School of Paediatrics and Child Health, University of Western Australia, Perth, Western Australia</nlm:aff></affiliation><affiliation><nlm:aff id="I9">Institute for Immunology and Infectious Diseases, Murdoch University, Perth, Western Australia</nlm:aff></affiliation></author><author><name sortKey="Weeramanthri, Tarun" sort="Weeramanthri, Tarun" uniqKey="Weeramanthri T" first="Tarun" last="Weeramanthri">Tarun Weeramanthri</name><affiliation><nlm:aff id="I10">Office of Population Health Genomics, Public Health and Clinical Services Division, Department of Health, Government of Western Australia, Perth, Western Australia</nlm:aff></affiliation></author><author><name sortKey="Dawkins, Hugh" sort="Dawkins, Hugh" uniqKey="Dawkins H" first="Hugh" last="Dawkins">Hugh Dawkins</name><affiliation><nlm:aff id="I1">Centre for Comparative Genomics, Murdoch University, Perth 6150, Western Australia</nlm:aff></affiliation><affiliation><nlm:aff id="I10">Office of Population Health Genomics, Public Health and Clinical Services Division, Department of Health, Government of Western Australia, Perth, Western Australia</nlm:aff></affiliation><affiliation><nlm:aff id="I11">School of Pathology & Laboratory Medicine, University of Western Australia, Perth, Western Australia</nlm:aff></affiliation><affiliation><nlm:aff id="I12">Curtin Health Innovation Research Institute, Curtin University of Technology, Perth, Western Australia</nlm:aff></affiliation></author><author><name sortKey="Hunter, Adam" sort="Hunter, Adam" uniqKey="Hunter A" first="Adam" last="Hunter">Adam Hunter</name><affiliation><nlm:aff id="I1">Centre for Comparative Genomics, Murdoch University, Perth 6150, Western Australia</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">24484969</idno><idno type="pmc">3917533</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917533</idno><idno type="RBID">PMC:3917533</idno><idno type="doi">10.1186/1751-0473-9-4</idno><date when="2014">2014</date><idno type="wicri:Area/Pmc/Corpus">001260</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001260</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Correction: Dispelling myths about rare disease registry system development</title><author><name sortKey="Bellgard, Matthew" sort="Bellgard, Matthew" uniqKey="Bellgard M" first="Matthew" last="Bellgard">Matthew Bellgard</name><affiliation><nlm:aff id="I1">Centre for Comparative Genomics, Murdoch University, Perth 6150, Western Australia</nlm:aff></affiliation></author><author><name sortKey="Beroud, Christophe" sort="Beroud, Christophe" uniqKey="Beroud C" first="Christophe" last="Beroud">Christophe Beroud</name><affiliation><nlm:aff id="I2">Faculté de Médecine de la Timone, INSERM UMR 910, Aix-Marseille Université, Marseille, France</nlm:aff></affiliation><affiliation><nlm:aff id="I3">AP-HM, Département de Génétique Médicale, Hôpital d’enfants Timone, Marseille, France</nlm:aff></affiliation></author><author><name sortKey="Parkinson, Kay" sort="Parkinson, Kay" uniqKey="Parkinson K" first="Kay" last="Parkinson">Kay Parkinson</name><affiliation><nlm:aff id="I4">Alstrom Syndrome, 49 Southfield Ave, Paignton S, Devon TQ3 1LH, UK</nlm:aff></affiliation></author><author><name sortKey="Harris, Tess" sort="Harris, Tess" uniqKey="Harris T" first="Tess" last="Harris">Tess Harris</name><affiliation><nlm:aff id="I5">Polycystic Kidney Disease Charity (UK), PKD International, Ciliopathy Alliance, London, UK</nlm:aff></affiliation></author><author><name sortKey="Ayme, Segolene" sort="Ayme, Segolene" uniqKey="Ayme S" first="Segolene" last="Ayme">Segolene Ayme</name><affiliation><nlm:aff id="I6">INSERM US14, ORPHANET 96 rue Didot, Paris 75014, France</nlm:aff></affiliation></author><author><name sortKey="Baynam, Gareth" sort="Baynam, Gareth" uniqKey="Baynam G" first="Gareth" last="Baynam">Gareth Baynam</name><affiliation><nlm:aff id="I7">Genetic Services of Western Australia, King Edward Memorial Hospital, Perth, Western Australia</nlm:aff></affiliation><affiliation><nlm:aff id="I8">School of Paediatrics and Child Health, University of Western Australia, Perth, Western Australia</nlm:aff></affiliation><affiliation><nlm:aff id="I9">Institute for Immunology and Infectious Diseases, Murdoch University, Perth, Western Australia</nlm:aff></affiliation></author><author><name sortKey="Weeramanthri, Tarun" sort="Weeramanthri, Tarun" uniqKey="Weeramanthri T" first="Tarun" last="Weeramanthri">Tarun Weeramanthri</name><affiliation><nlm:aff id="I10">Office of Population Health Genomics, Public Health and Clinical Services Division, Department of Health, Government of Western Australia, Perth, Western Australia</nlm:aff></affiliation></author><author><name sortKey="Dawkins, Hugh" sort="Dawkins, Hugh" uniqKey="Dawkins H" first="Hugh" last="Dawkins">Hugh Dawkins</name><affiliation><nlm:aff id="I1">Centre for Comparative Genomics, Murdoch University, Perth 6150, Western Australia</nlm:aff></affiliation><affiliation><nlm:aff id="I10">Office of Population Health Genomics, Public Health and Clinical Services Division, Department of Health, Government of Western Australia, Perth, Western Australia</nlm:aff></affiliation><affiliation><nlm:aff id="I11">School of Pathology & Laboratory Medicine, University of Western Australia, Perth, Western Australia</nlm:aff></affiliation><affiliation><nlm:aff id="I12">Curtin Health Innovation Research Institute, Curtin University of Technology, Perth, Western Australia</nlm:aff></affiliation></author><author><name sortKey="Hunter, Adam" sort="Hunter, Adam" uniqKey="Hunter A" first="Adam" last="Hunter">Adam Hunter</name><affiliation><nlm:aff id="I1">Centre for Comparative Genomics, Murdoch University, Perth 6150, Western Australia</nlm:aff></affiliation></author></analytic><series><title level="j">Source Code for Biology and Medicine</title><idno type="eISSN">1751-0473</idno><imprint><date when="2014">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Bellgard, M" uniqKey="Bellgard M">M Bellgard</name></author><author><name sortKey="Beroud, C" uniqKey="Beroud C">C Beroud</name></author><author><name sortKey="Parkinson, K" uniqKey="Parkinson K">K Parkinson</name></author><author><name sortKey="Harris, T" uniqKey="Harris T">T Harris</name></author><author><name sortKey="Ayme, S" uniqKey="Ayme S">S Ayme</name></author><author><name sortKey="Baynam, G" uniqKey="Baynam G">G Baynam</name></author><author><name sortKey="Weeramanthri, T" uniqKey="Weeramanthri T">T Weeramanthri</name></author><author><name sortKey="Dawkins, H" uniqKey="Dawkins H">H Dawkins</name></author><author><name sortKey="Hunter, A" uniqKey="Hunter A">A Hunter</name></author></analytic></biblStruct></listBibl></div1></back></TEI><pmc article-type="correction" xml:lang="en"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Source Code Biol Med</journal-id><journal-id journal-id-type="iso-abbrev">Source Code Biol Med</journal-id><journal-title-group><journal-title>Source Code for Biology and Medicine</journal-title></journal-title-group><issn pub-type="epub">1751-0473</issn><publisher><publisher-name>BioMed Central</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">24484969</article-id><article-id pub-id-type="pmc">3917533</article-id><article-id pub-id-type="publisher-id">1751-0473-9-4</article-id><article-id pub-id-type="doi">10.1186/1751-0473-9-4</article-id><article-categories><subj-group subj-group-type="heading"><subject>Correction</subject></subj-group></article-categories><title-group><article-title>Correction: Dispelling myths about rare disease registry system development</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes" id="A1"><name><surname>Bellgard</surname><given-names>Matthew</given-names></name><xref ref-type="aff" rid="I1">1</xref><email>mbellgard@ccg.murdoch.edu.au</email></contrib><contrib contrib-type="author" id="A2"><name><surname>Beroud</surname><given-names>Christophe</given-names></name><xref ref-type="aff" rid="I2">2</xref><xref ref-type="aff" rid="I3">3</xref><email>christophe.beroud@inserm.fr</email></contrib><contrib contrib-type="author" id="A3"><name><surname>Parkinson</surname><given-names>Kay</given-names></name><xref ref-type="aff" rid="I4">4</xref><email>kay.parkinson@alstrom.org.uk</email></contrib><contrib contrib-type="author" id="A4"><name><surname>Harris</surname><given-names>Tess</given-names></name><xref ref-type="aff" rid="I5">5</xref><email>tess.harris@pkdcharity.org.uk</email></contrib><contrib contrib-type="author" id="A5"><name><surname>Ayme</surname><given-names>Segolene</given-names></name><xref ref-type="aff" rid="I6">6</xref><email>segolene.ayme@inserm.fr</email></contrib><contrib contrib-type="author" id="A6"><name><surname>Baynam</surname><given-names>Gareth</given-names></name><xref ref-type="aff" rid="I7">7</xref><xref ref-type="aff" rid="I8">8</xref><xref ref-type="aff" rid="I9">9</xref><email>Gareth.Baynam@health.wa.gov.au</email></contrib><contrib contrib-type="author" id="A7"><name><surname>Weeramanthri</surname><given-names>Tarun</given-names></name><xref ref-type="aff" rid="I10">10</xref><email>Tarun.Weeramanthri@health.wa.gov.au</email></contrib><contrib contrib-type="author" id="A8"><name><surname>Dawkins</surname><given-names>Hugh</given-names></name><xref ref-type="aff" rid="I1">1</xref><xref ref-type="aff" rid="I10">10</xref><xref ref-type="aff" rid="I11">11</xref><xref ref-type="aff" rid="I12">12</xref><email>Hugh.Dawkins@health.wa.gov.au</email></contrib><contrib contrib-type="author" id="A9"><name><surname>Hunter</surname><given-names>Adam</given-names></name><xref ref-type="aff" rid="I1">1</xref><email>ahunter@ccg.murdoch.edu.au</email></contrib></contrib-group><aff id="I1"><label>1</label>Centre for Comparative Genomics, Murdoch University, Perth 6150, Western Australia</aff><aff id="I2"><label>2</label>Faculté de Médecine de la Timone, INSERM UMR 910, Aix-Marseille Université, Marseille, France</aff><aff id="I3"><label>3</label>AP-HM, Département de Génétique Médicale, Hôpital d’enfants Timone, Marseille, France</aff><aff id="I4"><label>4</label>Alstrom Syndrome, 49 Southfield Ave, Paignton S, Devon TQ3 1LH, UK</aff><aff id="I5"><label>5</label>Polycystic Kidney Disease Charity (UK), PKD International, Ciliopathy Alliance, London, UK</aff><aff id="I6"><label>6</label>INSERM US14, ORPHANET 96 rue Didot, Paris 75014, France</aff><aff id="I7"><label>7</label>Genetic Services of Western Australia, King Edward Memorial Hospital, Perth, Western Australia</aff><aff id="I8"><label>8</label>School of Paediatrics and Child Health, University of Western Australia, Perth, Western Australia</aff><aff id="I9"><label>9</label>Institute for Immunology and Infectious Diseases, Murdoch University, Perth, Western Australia</aff><aff id="I10"><label>10</label>Office of Population Health Genomics, Public Health and Clinical Services Division, Department of Health, Government of Western Australia, Perth, Western Australia</aff><aff id="I11"><label>11</label>School of Pathology & Laboratory Medicine, University of Western Australia, Perth, Western Australia</aff><aff id="I12"><label>12</label>Curtin Health Innovation Research Institute, Curtin University of Technology, Perth, Western Australia</aff><pub-date pub-type="collection"><year>2014</year></pub-date><pub-date pub-type="epub"><day>31</day><month>1</month><year>2014</year></pub-date><volume>9</volume><fpage>4</fpage><lpage>4</lpage><history><date date-type="received"><day>17</day><month>1</month><year>2014</year></date><date date-type="accepted"><day>28</day><month>1</month><year>2014</year></date></history><permissions><copyright-statement>Copyright © 2014 Bellgard et al.; licensee BioMed Central Ltd.</copyright-statement><copyright-year>2014</copyright-year><copyright-holder>Bellgard et al.; licensee BioMed Central Ltd.</copyright-holder><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/2.0"><license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/2.0">http://creativecommons.org/licenses/by/2.0</ext-link>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/publicdomain/zero/1.0/">http://creativecommons.org/publicdomain/zero/1.0/</ext-link>) applies to the data made available in this article, unless otherwise stated.</license-p></license></permissions><self-uri xlink:href="http://www.scfbm.org/content/9/1/4"></self-uri><related-article related-article-type="corrected-article" id="d33e6" vol="8" page="21" xlink:href="24131574" ext-link-type="pubmed"></related-article></article-meta></front><body><sec><title>Correction</title><p>After publication of this work [<xref ref-type="bibr" rid="B1">1</xref>], we noted that we inadvertently failed to include important Acknowledgments in our final version of the manuscript. Please see below the modification:</p></sec><sec><title>Acknowledgements</title><p>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></sec></body><back><ref-list><ref id="B1"><mixed-citation publication-type="journal"><name><surname>Bellgard</surname><given-names>M</given-names></name><name><surname>Beroud</surname><given-names>C</given-names></name><name><surname>Parkinson</surname><given-names>K</given-names></name><name><surname>Harris</surname><given-names>T</given-names></name><name><surname>Ayme</surname><given-names>S</given-names></name><name><surname>Baynam</surname><given-names>G</given-names></name><name><surname>Weeramanthri</surname><given-names>T</given-names></name><name><surname>Dawkins</surname><given-names>H</given-names></name><name><surname>Hunter</surname><given-names>A</given-names></name><article-title>Dispelling myths about rare disease registry system development</article-title><source>Source Code Biol Med</source><year>2013</year><volume>8</volume><fpage>21</fpage><pub-id pub-id-type="doi">10.1186/1751-0473-8-21</pub-id><pub-id pub-id-type="pmid">24131574</pub-id></mixed-citation></ref></ref-list></back></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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