Correction to: Establishing a core outcome set for mucopolysaccharidoses (MPS) in children: study protocol for a rapid literature review, candidate outcomes survey, and Delphi surveys

• Alison H. Howie,
• Kylie Tingley,
• Michal Inbar-Feigenberg,
• John J. Mitchell,
• Nancy J. Butcher,
• Martin Offringa,
• Maureen Smith,
• Kim Angel,
• Jenifer Gentle,
• Alexandra Wyatt,
• Philippe M. Campeau,
• Alicia Chan,
• Pranesh Chakraborty,
• Farah El Turk,
• Eva Mamak,
• Aizeddin Mhanni,
• Becky Skidmore,
• Rebecca Sparkes,
• Sylvia Stockler,
• Beth K. Potter,
• in collaboration with the INFORM RARE Network

Affiliations

Alison H. Howie

School of Epidemiology and Public Health, University of Ottawa

Kylie Tingley

School of Epidemiology and Public Health, University of Ottawa

Michal Inbar-Feigenberg

The Hospital for Sick Children

John J. Mitchell

McGill University Health Centre

Nancy J. Butcher

Child Health Evaluative Sciences, The Hospital for Sick Children Research Institute

Martin Offringa

The Hospital for Sick Children

Maureen Smith

Patient Partner, Canadian Organization for Rare Disorders

Kim Angel

Canadian MPS Society

Jenifer Gentle

Patient/Family Partner

Alexandra Wyatt

Canadian MPS Society

Philippe M. Campeau

Department of Pediatrics, CHU Sainte-Justine and Université de Montréal

Alicia Chan

Department of Medical Genetics, University of Alberta

Pranesh Chakraborty

Children’s Hospital of Eastern Ontario

Farah El Turk

McGill University Health Centre

Eva Mamak

Department of Psychology, The Hospital for Sick Children

Aizeddin Mhanni

Department of Pediatrics and Child Health, and Department of Biochemistry and Medical Genetics, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba

Becky Skidmore

Ottawa Hospital Research Institute

Rebecca Sparkes

Department of Medical Genetics and Pediatrics, University of Calgary

Sylvia Stockler

Biochemical Diseases, BC Children’s Hospital

Beth K. Potter

School of Epidemiology and Public Health, University of Ottawa

in collaboration with the INFORM RARE Network