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Erratum to: Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey
Authors:Tracy A. Briggs  Gillian I. Rice  Navid Adib  Lesley Ades  Stephane Barete  Kannan Baskar  Veronique Baudouin  Ayse N. Cebeci  Philippe Clapuyt  David Coman  Lien De Somer  Yael Finezilber  Moshe Frydman  Ayla Guven  Sébastien Heritier  Daniela Karall  Muralidhar L. Kulkarni  Pierre Lebon  David Levitt  Martine Le Merrer  Agnes Linglart  John H. Livingston  Vincent Navarro  Ericka Okenfuss  Anne Puel  Nicole Revencu  Sabine Scholl-Bürgi  Marina Vivarelli  Carine Wouters  Brigitte Bader-Meunier  Yanick J. Crow
Affiliation:1.Manchester Centre for Genomic Medicine, Institute of Human Development, Faculty of Medical and Human Sciences,University of Manchester,Manchester,UK;2.St Mary’s Hospital, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre,Manchester,UK;3.Department of Rheumatology,The Lady Cilento Children’s Hospital,Brisbane,Australia;4.Department of Clinical Genetics,The Children’s Hospital at Westmead,Sydney,Australia;5.Discipline of Paedatrics and Child Health,The University of Sydney,Sydney,Australia;6.Dermatology Department,Pitie-Salpetriere Hospital,Paris,France;7.Creighton University,Omaha,USA;8.Pediatric Nephrology Department,Robert Debré University Hospital– APHP,Paris,France;9.Goztepe Educational and Research Hospital Pediatric Endocrinology Clinic,Istanbul,Türkiye;10.Pediatric Imaging Unit, Cliniques universitaires Saint-Luc,Université catholique de Louvain,Brussels,Belgium;11.Neuroscience Department,The Lady Cilento Children’s Hospital,Brisbane,Australia;12.School of Medicine,Griffith University,Gold Coast,Australia;13.Pediatric Rheumatology, Department of Pediatrics,University Hospitals Leuven,Leuven,Belgium;14.Danek Gertner Institute of Human Genetics,Chaim Sheba Medical Center,Tel Aviv,Israel;15.Sackler School of Medicine,Tel Aviv University,Tel Aviv,Israel;16.Amasya University Medical Faculty,Department of Pediatric Endocrinology,Istanbul,Türkiye;17.Department of Pediatric Hematology and Oncology,Trousseau Hospital, Assistance Publique–H?pitaux de Paris (APHP),Paris,France;18.Clinic for Pediatrics I, Inherited Metabolic Disorders,Medical University of Innsbruck,Innsbruck,Austria;19.J. J. M. Medical College,Davangere,India;20.Service de Virologie,AP-HP H?pital Cochin,Paris,France;21.Department of Paediatrics,The Lady Cilento Children’s Hospital,Brisbane,Australia;22.Centre de Référence des Maladies Osseuses Constitutionnelles et Institut Imagine,Paris,France;23.APHP, Bicêtre Paris Sud, Department of Pediatric Endocrinology and Diabetology for Children,Le Kremlin Bicêtre,France;24.Reference Center for Rare Disorders of the Mineral Metabolism and Plateforme d’expertise Paris Sud Maladies Rares, APHP,Le Kremlin Bicêtre,France;25.Department of Paediatric Neurology,Leeds Teaching Hospitals NHS Trust,Leeds,UK;26.Epilepsy Unit,Pitie-Salpetriere Hospital,Paris,France;27.Kaiser Permanente – Genetics,Sacramento,USA;28.Génétique Humaine des Maladies Infectieuses, INSERM UMR 1163,Université Paris Descartes Sorbonne Paris Cité, Institut Imagine,Paris,France;29.Centre for Human Genetics, Cliniques universitaires Saint-Luc,Université catholique de Louvain,Brussels,Belgium;30.Division of Nephrology,IRCCS Bambino Gesu’ Pediatric Hospital,Rome,Italy;31.Department of Microbiology and Immunology, Pediatric Immunology, KU Leuven,University of Leuven,Leuven,Belgium;32.Pediatric Immunology and Rheumatology Unit,H?pital Necker, APHP,Paris,France;33.Institut Imagine,Paris,France;34.Laboratory of Neurogenetics and Neuroinflammation, Institut Imagine,Paris,France
Abstract:
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