| Authors: |
Fuchs SA; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands. S.Fuchs@umcutrecht.nl., Schene IF; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands., Kok G; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands., Jansen JM; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands., Nikkels PGJ; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands., van Gassen KLI; Department of Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands., Terheggen-Lagro SWJ; Department of Pediatric Pulmonology, Academic Medical Center Amsterdam, Amsterdam, The Netherlands., van der Crabben SN; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands., Hoeks SE; Department of Neonatology, University Medical Center Utrecht, Utrecht, The Netherlands., Niers LEM; Department of Pediatrics, Maxima Medical Centre Veldhoven, Veldhoven, The Netherlands., Wolf NI; Department of Child Neurology, VU University Medical Center, Amsterdam, The Netherlands., de Vries MC; Nijmegen Centre for Mitochondrial Disorders at Department of Pediatrics, Radboud University Nijmegen Centre, Nijmegen, The Netherlands., Koolen DA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., Houwen RHJ; Division of Pediatric Gastroenterology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands., Mulder MF; Department of Pediatrics, VU University Medical Center, Amsterdam, The Netherlands., van Hasselt PM; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands. |