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Open Access
Peer-reviewed
Research Article
Uncovering Genomic Causes of Co-Morbidity in Epilepsy: Gene-Driven Phenotypic Characterization of Rare Microdeletions
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Dalia Kasperavičiūtė,
Affiliation Department of Clinical and Experimental Epilepsy, University College London Institute of Neurology, London, United Kingdom
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Claudia B. Catarino,
Affiliations Department of Clinical and Experimental Epilepsy, University College London Institute of Neurology, London, United Kingdom, National Society for Epilepsy, Chalfont-St-Peter, Bucks, United Kingdom
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Krishna Chinthapalli,
Affiliation Department of Clinical and Experimental Epilepsy, University College London Institute of Neurology, London, United Kingdom
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Lisa M. S. Clayton,
Affiliation Department of Clinical and Experimental Epilepsy, University College London Institute of Neurology, London, United Kingdom
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Maria Thom,
Affiliation Department of Clinical and Experimental Epilepsy, University College London Institute of Neurology, London, United Kingdom
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Lillian Martinian,
Affiliation Department of Clinical and Experimental Epilepsy, University College London Institute of Neurology, London, United Kingdom
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Hannah Cohen,
Affiliation Department of Haematology, University College London and University College London Hospitals NHS Foundation Trust, London, United Kingdom
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Shazia Adalat,
Affiliation Renal Unit, University College London Institute of Child Health and Great Ormond Street Hospital NHS Trust, London, United Kingdom
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Detlef Bockenhauer,
Affiliation Renal Unit, University College London Institute of Child Health and Great Ormond Street Hospital NHS Trust, London, United Kingdom
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Simon A. Pope,
Affiliation Neurometabolic Unit, National Hospital for Neurology and Neurosurgery, London, United Kingdom
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Nicholas Lench,
Affiliation North East Thames Regional Genetics Service, Great Ormond Street Hospital for Children, London, United Kingdom
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Martin Koltzenburg,
Affiliations Sobell Department of Motor Neuroscience and Movement Disorders, University College London Institute of Neurology, London, United Kingdom, MRC Centre for Neuromuscular Diseases, National Hospital for Neurology and Neurosurgery, London, United Kingdom
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John S. Duncan,
Affiliations Department of Clinical and Experimental Epilepsy, University College London Institute of Neurology, London, United Kingdom, National Society for Epilepsy, Chalfont-St-Peter, Bucks, United Kingdom
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Peter Hammond,
Affiliation Molecular Medicine Unit, University College London Institute of Child Health, London, United Kingdom
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Raoul C. M. Hennekam,
Affiliation Department of Pediatrics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands
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John M. Land,
Affiliation Neurometabolic Unit, National Hospital for Neurology and Neurosurgery, London, United Kingdom
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Sanjay M. Sisodiya
* E-mail: s.sisodiya@ion.ucl.ac.uk
Affiliations Department of Clinical and Experimental Epilepsy, University College London Institute of Neurology, London, United Kingdom, National Society for Epilepsy, Chalfont-St-Peter, Bucks, United Kingdom
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Uncovering Genomic Causes of Co-Morbidity in Epilepsy: Gene-Driven Phenotypic Characterization of Rare Microdeletions
- Dalia Kasperavičiūtė,
- Claudia B. Catarino,
- Krishna Chinthapalli,
- Lisa M. S. Clayton,
- Maria Thom,
- Lillian Martinian,
- Hannah Cohen,
- Shazia Adalat,
- Detlef Bockenhauer,
- Simon A. Pope
- Published: August 17, 2011
- https://doi.org/10.1371/journal.pone.0023182