Article Information
vol. 5 no. 2
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History
- Received November 2, 2018
- Accepted February 28, 2019
- Published online April 26, 2019.
Copyright & Usage
Copyright ©ERS 2019 This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.
Author Information
- 1Division of Respiratory Medicine, BC Children's Hospital, Vancouver, BC, Canada
- 2Dept of Paediatrics, University of British Columbia, Vancouver, BC, Canada
- 3Dept of Paediatrics, University of Toronto, Toronto, ON, Canada
- 4Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON, Canada
- 5Dept of Clinical Genetics, Addenbrooke's Treatment Centre, Cambridge University Hospitals, Cambridge, UK
- 6Division of Pathology, Dept of Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, ON, Canada
- 7Division of Respiratory Medicine, The Hospital for Sick Children, Toronto, ON, Canada
- 8Institute of Health Policy, Management and Education, University of Toronto, Toronto, ON, Canada
- 9Child Health Evaluative Sciences, The Hospital for Sick Children Research Institute, Toronto, ON, Canada
- Sharon D. Dell, Division of Respiratory Medicine, Room 4543, The Hospital for Sick Children, 555 University Ave, Toronto, ON, M5G 1X8, Canada. E-mail: sharon.dell{at}sickkids.ca
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Vol 5 Issue 2
Table of Contents
Prolidase deficiency diagnosed by whole exome sequencing in a child with pulmonary capillaritis
