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Dominant‐negative effects of KCNQ2 mutations are associated with epileptic encephalopathy
Authors:Gökce Orhan MD  Merle Bock MSc  Dorien Schepers MSc  Elena I. Ilina MSc  Stephanie Nadine Reichel BSc  Heidi Löffler  Nicole Jezutkovic  Sarah Weckhuysen MD  Simone Mandelstam MB  ChB  Arvid Suls PhD  Timm Danker PhD  Elke Guenther PhD  Ingrid E. Scheffer MBBS  PhD  Peter De Jonghe MD  PhD  Holger Lerche MD  Snezana Maljevic PhD
Affiliation:1. Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany;2. Neurogenetics Group, Department of Molecular Genetics, VIB, Antwerp, Belgium;3. Laboratory of Neurogenetics, Institute Born‐Bunge, University of Antwerp, Antwerp, Belgium;4. Epilepsy Center Kempenhaeghe, Oosterhout, the Netherlands;5. Florey Institute of Neuroscience and Mental Health, Melbourne, Australia;6. Departments of Pediatrics and Radiology, University of Melbourne, Melbourne, Australia;7. Institute at University of Tübingen, University of Tübingen, Reutlingen, Germany;8. University of Melbourne, Austin Health and Royal Children's Hospital, Melbourne, Australia;9. Division of Neurology, Antwerp University Hospital, Antwerp, Belgium
Abstract:
Keywords:
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