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NADH:Q1 oxidoreductase deficiency without lactic acidosis in a patient with leigh syndrome: Implications for the diagnosis of inborn errors of the respiratory chain
Authors:F A Wijburg  R J A Wanders  E M van Lie Peters  G D Vos  H G Loggers  P A Bolhuis  N H Herzberg  W Ruitenbeek  A van Wilsem  R ten Houten  P G Barth
Institution:(1) Department of Paediatrics, University Hospital Amsterdam (AMC), Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands;(2) Department of Neurology, University Hospital Amsterdam (AMC), Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands;(3) Department of Paediatrics, University of Nijmegen, 6500 HB Nijmegen, The Netherlands;(4) Department of Paediatrics, Medical Centre, 1815 JD Alkmaar, The Netherlands;(5) Department of Neurology, Medical Centre, 1815 JD Alkmaar, The Netherlands
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