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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 |
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| 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 |
| Affiliation: | (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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