| Authors: |
Awamleh Z; Genetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON M5G 1X8, Canada., Chen A; Genetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON M5G 1X8, Canada., Choufani S; Genetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON M5G 1X8, Canada., Rots D; Clinical genetics department, Erasmus MC, Rotterdam, The Netherlands., Ko JM; Department of Pediatrics, Rare Disease Center, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea., Armour CM; Regional Genetics Program, Children's Hospital of Eastern Ontario, and Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada., Nowaczyk MJM; Division of Clinical and Metabolic Genetics, Department of Pediatrics, McMaster Children's Hospital, McMaster University, Hamilton, Ontario, Canada., Hurst ACE; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL, USA., Gibson WT; Department of Medical Genetics, University of British Columbia, and BC Children's Hospital Research Institute, Vancouver, British Columbia., Misceo D; Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway., Frengen E; Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway., Strømme P; Division of Pediatric and Adolescent Medicine, Oslo University Hospital and University of Oslo, Oslo, Norway., Soliani L; IRCCS Istituto delle Scienze Neurologiche di Bologna, U.O.C. Neuropsichiatria dell'età Pediatrica, 40138 Bologna, Italy., McNiven V; Division of Clinical and Metabolic Genetics, Department of Pediatrics, McMaster Children's Hospital, McMaster University, Hamilton, Ontario, Canada., Alkhunaizi E; Division of Clinical and Metabolic Genetics, Department of Pediatrics, the Hospital for Sick Children, University of Toronto, Toronto, ON M5G 1X8, Canada., Invernizzi F; Medical Genetics and Neurogenetics Unit, Movement Disorders Diagnostic Section, Fondazione Irccs Istituto Neurologico Carlo Besta, 20133 Milan, Italy., Fernandes S; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, EPE, Coimbra, Portugal; Familial Risk Clinic, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisboa, Portugal., Sousa S; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, EPE, Coimbra, Portugal., Amoros I; Department of Pediatrics, Hospital Punta De Europa, Algeciras, Spain., Scherer SW; Genetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON M5G 1X8, Canada; McLaughlin Centre and Department of Molecular Genetics, University of Toronto, Ontario, Canada., Kwint M; Department of Human Genetics, Radboud university medical center, Donders Institute for Brain, Cognition, and Behavior, Nijmegen, The Netherlands., Bienvenu T; Université Paris Cité, Institut of Psychiatry and Neuroscience of Paris (IPNP), INSERM U1266, Equipe Gorwood/Ramoz, 75014, Paris, France., Garavaglia BM; Medical Genetics and Neurogenetics Unit, Movement Disorders Diagnostic Section, Fondazione Irccs Istituto Neurologico Carlo Besta, 20133 Milan, Italy., Ortigoza-Escobar JD; Movement Disorders Unit, Institut de Recerca Sant Joan de Déu, CIBERER-ISCIII and European Reference Network for Rare Neurological Diseases (ERN-RND), Barcelona, Spain., Weksberg R; Genetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON M5G 1X8, Canada; Division of Clinical and Metabolic Genetics, Department of Pediatrics, the Hospital for Sick Children, University of Toronto, Toronto, ON M5G 1X8, Canada. Electronic address: rweksb@sickkids.ca. |
