Erratum to: Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey

Briggs, Tracy A.; Rice, Gillian I.; Adib, Navid; Ades, Lesley; Barete, Stephane; Baskar, Kannan; Baudouin, Veronique; Cebeci, Ayse N.; Clapuyt, Philippe; Coman, David; De Somer, Lien; Finezilber, Yael; Frydman, Moshe; Guven, Ayla; Heritier, Sébastien; Karall, Daniela; Kulkarni, Muralidhar L.; Lebon, Pierre; Levitt, David; Le Merrer, Martine; Linglart, Agnes; Livingston, John H.; Navarro, Vincent; Okenfuss, Ericka; Puel, Anne; Revencu, Nicole; Scholl-Bürgi, Sabine; Vivarelli, Marina; Wouters, Carine; Bader-Meunier, Brigitte; Crow, Yanick J.

doi:10.1007/s10875-016-0287-0

Erratum to: Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey

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Published: 29 April 2016

Volume 36, pages 529–530, (2016)
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Erratum to: Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey

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Tracy A. Briggs^1,2,
Gillian I. Rice¹,
Navid Adib³,
Lesley Ades^4,5,
Stephane Barete⁶,
Kannan Baskar⁷,
Veronique Baudouin⁸,
Ayse N. Cebeci⁹,
Philippe Clapuyt¹⁰,
David Coman^11,12,
Lien De Somer¹³,
Yael Finezilber¹⁴,
Moshe Frydman^14,15,
Ayla Guven^9,16,
Sébastien Heritier¹⁷,
Daniela Karall¹⁸,
Muralidhar L. Kulkarni¹⁹,
Pierre Lebon²⁰,
David Levitt²¹,
Martine Le Merrer²²,
Agnes Linglart^23,24,
John H. Livingston²⁵,
Vincent Navarro²⁶,
Ericka Okenfuss²⁷,
Anne Puel²⁸,
Nicole Revencu²⁹,
Sabine Scholl-Bürgi¹⁸,
Marina Vivarelli³⁰,
Carine Wouters³¹,
Brigitte Bader-Meunier^32,33 &
…
Yanick J. Crow^1,34

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The Original Article was published on 08 March 2016

Erratum to: J Clin Immunol. 2016 Apr;36(3):220–34

DOI 10.1007/s10875-016-0252-y

The original version of this article did not contain acknowledgements. These are presented below.

Acknowledgments

We sincerely thank the participating families for the use of genetic samples and clinical information. We also thank Dr Banan Musallam-Jabbour, Israel and Dr Giuseppina Ognisanti, Sicily for providing clinical data. TAB acknowledges funding support from the National Institute for Health Research, the Academy of Medical Sciences, the Wellcome Trust, Medical Research Council, British Heart Foundation, Arthritis Research UK, Prostate Cancer UK and the Royal College of Physicians and the National Institute for Health Research Manchester Musculoskeletal Biomedical Research Unit. The views expressed in this publication are those of the author(s) and not necessarily those of the NHS, the National Institute for Health Research or the Department of Health. Y.J.C. acknowledges the European Research Council (GA 309449: Fellowship), and a state subsidy managed by the National Research Agency (France) under the “Investments for the Future” program bearing the reference ANR-10-IAHU-01. The authors would like to thank the National Heart, Lung, and Blood Institute (NHLBI) Exome Sequencing Project (ESP) database.

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Authors and Affiliations

Manchester Centre for Genomic Medicine, Institute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, Manchester, UK
Tracy A. Briggs, Gillian I. Rice & Yanick J. Crow
St Mary’s Hospital, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK
Tracy A. Briggs
Department of Rheumatology, The Lady Cilento Children’s Hospital, Brisbane, Australia
Navid Adib
Department of Clinical Genetics, The Children’s Hospital at Westmead, Sydney, Australia
Lesley Ades
Discipline of Paedatrics and Child Health, The University of Sydney, Sydney, Australia
Lesley Ades
Dermatology Department, Pitie-Salpetriere Hospital, Paris, France
Stephane Barete
Creighton University, 2500 California Plaza, Omaha, NE, 68178, USA
Kannan Baskar
Pediatric Nephrology Department, Robert Debré University Hospital– APHP, 48 boulevard Sérurier, 75019, Paris, France
Veronique Baudouin
Goztepe Educational and Research Hospital Pediatric Endocrinology Clinic, Istanbul, Türkiye
Ayse N. Cebeci & Ayla Guven
Pediatric Imaging Unit, Cliniques universitaires Saint-Luc, Université catholique de Louvain, Brussels, Belgium
Philippe Clapuyt
Neuroscience Department, The Lady Cilento Children’s Hospital, Brisbane, Australia
David Coman
School of Medicine, Griffith University, Gold Coast, Australia
David Coman
Pediatric Rheumatology, Department of Pediatrics, University Hospitals Leuven, B-3000, Leuven, Belgium
Lien De Somer
Danek Gertner Institute of Human Genetics, Chaim Sheba Medical Center, Tel Aviv, Israel
Yael Finezilber & Moshe Frydman
Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel
Moshe Frydman
Amasya University Medical Faculty, Department of Pediatric Endocrinology, Istanbul, Türkiye
Ayla Guven
Department of Pediatric Hematology and Oncology, Trousseau Hospital, Assistance Publique–Hôpitaux de Paris (APHP), Paris, France
Sébastien Heritier
Clinic for Pediatrics I, Inherited Metabolic Disorders, Medical University of Innsbruck, Anichstr. 35, A-6020, Innsbruck, Austria
Daniela Karall & Sabine Scholl-Bürgi
J. J. M. Medical College, Davangere, Karnataka, 577004, India
Muralidhar L. Kulkarni
Service de Virologie, AP-HP Hôpital Cochin, Paris, France
Pierre Lebon
Department of Paediatrics, The Lady Cilento Children’s Hospital, Brisbane, Australia
David Levitt
Centre de Référence des Maladies Osseuses Constitutionnelles et Institut Imagine, Hopital Necker 149 rue de Sevres, 75015, Paris, France
Martine Le Merrer
APHP, Bicêtre Paris Sud, Department of Pediatric Endocrinology and Diabetology for Children, 94270, Le Kremlin Bicêtre, France
Agnes Linglart
Reference Center for Rare Disorders of the Mineral Metabolism and Plateforme d’expertise Paris Sud Maladies Rares, APHP, 94270, Le Kremlin Bicêtre, France
Agnes Linglart
Department of Paediatric Neurology, Leeds Teaching Hospitals NHS Trust, Leeds, UK
John H. Livingston
Epilepsy Unit, Pitie-Salpetriere Hospital, Paris, France
Vincent Navarro
Kaiser Permanente – Genetics, 1650 Response Rd, Sacramento, CA, 95815, USA
Ericka Okenfuss
Génétique Humaine des Maladies Infectieuses, INSERM UMR 1163, Université Paris Descartes Sorbonne Paris Cité, Institut Imagine, Pièce 421-B1, 24 boulevard du Montparnasse, 75015, Paris, France
Anne Puel
Centre for Human Genetics, Cliniques universitaires Saint-Luc, Université catholique de Louvain, Brussels, Belgium
Nicole Revencu
Division of Nephrology, IRCCS Bambino Gesu’ Pediatric Hospital, Rome, Italy
Marina Vivarelli
Department of Microbiology and Immunology, Pediatric Immunology, KU Leuven, University of Leuven, Leuven, Belgium
Carine Wouters
Pediatric Immunology and Rheumatology Unit, Hôpital Necker, APHP, Paris, France
Brigitte Bader-Meunier
Institut Imagine, Paris, France
Brigitte Bader-Meunier
Laboratory of Neurogenetics and Neuroinflammation, Institut Imagine, 24 boulevard du Montparnasse, 75015, Paris, France
Yanick J. Crow

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Tracy A. Briggs
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Gillian I. Rice
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Navid Adib
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Lesley Ades
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Stephane Barete
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Kannan Baskar
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Veronique Baudouin
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Ayse N. Cebeci
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Philippe Clapuyt
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David Coman
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Lien De Somer
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Yael Finezilber
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Moshe Frydman
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Ayla Guven
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Sébastien Heritier
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Daniela Karall
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Muralidhar L. Kulkarni
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Pierre Lebon
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David Levitt
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Martine Le Merrer
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Agnes Linglart
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John H. Livingston
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Vincent Navarro
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Ericka Okenfuss
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Anne Puel
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Nicole Revencu
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Correspondence to Tracy A. Briggs.

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The online version of the original article can be found at http://dx.doi.org/10.1007/s10875-016-0252-y.

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Briggs, T.A., Rice, G.I., Adib, N. et al. Erratum to: Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey. J Clin Immunol 36, 529–530 (2016). https://doi.org/10.1007/s10875-016-0287-0

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Published: 29 April 2016
Issue Date: July 2016
DOI: https://doi.org/10.1007/s10875-016-0287-0

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Erratum to: Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey

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