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Epilepsy due to PNPO mutations: Genotype, environment and treatment affect presentation and outcome

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第一作者: Mills,P.B.
作者单位: Neurosciences Unit, Great Ormond Street Hospital for Children, NHS Foundation Trust, London WC1N [1] Department of Medicine, Adult Genetics Clinic, University Health Network, 60 Murray Street, Toronto [2] Division of Child Neurology and Children's Research Centre (CRC), University Children's Hospital [3] Division of Metabolic Diseases, University Children's Hospital Zurich, Steinwiesstra?e 75, 8032 [4] Department of Clinical Neurophysiology, Great Ormond Street Hospital for Children, NHS Foundation [5] Department of Paediatrics, University of Naples Federico II, Naples, Italy [6] Neuropaediatric Unit, Astrid Lindgren Children's Hospital, 17176 Solna, Sweden [7] Hospital of Eastern Switzerland, Department of Child Neurology, Development and Rehabilitation, St [8] Clinical and Molecular Genetics Unit, UCL Institute of Child Health, 30 Guilford St, London WC1N [9] Department of Medical Translational Sciences, Section of Paediatrics, Università Federico II di [10] Department of Radiology, Great Ormond Street Hospital for Children, NHS Foundation Trust, London [11] Airedale NHS Foundation Trust, Skipton Road, Steeton, BD20 6TD, United Kingdom [12] Department of Child Neurology, VU University Medical Centre, Neuroscience Campus Amsterdam, 1007MB [13] Neurosciences Unit, Mater Children's Hospital, South Brisbane, QLD 4101, Australia [14] Department of Paediatrics, INSERM U954, Children's Hospital of Nancy, Allée du Morvan, Vandoeuvre [15] Fraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Dalnair St, Yorkhill [16] Leeds Children's Hospital, Clarendon Wing, Leeds General Infirmary, Leeds West Yorkshire LS1 3EX [17]
发布时间 2014-07-31
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Brain: A journal of neurology

Brain

2014年137卷5期

1350-1360页

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