| Authors: |
de Souza CFM; Hospital de Clinicas de Porto Alegre (HCPA), Casa dos Raros, Post Graduate Program in Child and Adolescent Health Federal University of Rio Grande do Sul (UFRGS), Porto Alegre, Brazil., Burton BK; Ann & Robert H. Lurie Children's Hospital of Chicago and Northwestern University Feinberg School of Medicine, Chicago, IL, USA., Campeau PM; CHU Sainte-Justine Research Center, Montreal, QC, Canada., Giugliani R; Federal University of Rio Grande do Sul (UFRGS), Hospital de Clinicas de Porto Alegre (HCPA), Dasa Genomics, and Casa dos Raros, Porto Alegre, Brazil., Guffon N; Reference Center for Inherited Metabolic Diseases, Hospices Civils de Lyon, France., Lampe C; University hospital of Gießen, Gießen, Lysosomal Unit, Center for Rare Diseases, Germany., Muschol N; International Center for Lysosomal Disorders (ICLD), University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Sivri S; Hacettepe University Children's Hospital, Ankara, Turkey., Solano M; Fundación Cardioinfantil, Bogotá, Colombia., Stepien KM; Salford Royal Hospital, Northern Care Alliance NHS Foundation Trust, Salford, UK. |
