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Neurogenetics
Original research
Adult phenotype of KCNQ2 encephalopathy

Authors

  • Stephanie Boets Neurology Department, University Hospital Antwerp, Antwerp, Belgium PubMed articlesGoogle scholar articles
  • Katrine M Johannesen Department of Epilepsy Genetics and Personalized Treatment, The Danish Epilepsy Centre Filadelfia, Dianalund, Denmark Institute for Regional Health Research, University of Southern Denmark, Odense, Denmark PubMed articlesGoogle scholar articles
  • Anne Destree Department of Human Genetics, Institute of Pathology and Genetics, Gosselies, Belgium PubMed articlesGoogle scholar articles
  • Filippo Manti Department of Human Neuroscience, University of Rome La Sapienza, Roma, Lazio, Italy PubMed articlesGoogle scholar articles
  • Georgia Ramantani Department of Neuropediatrics, University Children's Hospital, Zurich, Switzerland PubMed articlesGoogle scholar articles
  • Gaetan Lesca Department of Genetics, University Hospitals of Lyon, Lyon, France Neuroscience Research Center, Claude Bernard Lyon I University, Lyon, France PubMed articlesGoogle scholar articles
  • Laurent Vercueil Grenoble Institute of Neurosciences (GIN), University Grenoble Alpes, La Tronche, France PubMed articlesGoogle scholar articles
  • Mary Kay Koenig Department of Pediatrics, University of Texas McGovern Medical School, Houston, Texas, USA PubMed articlesGoogle scholar articles
  • Pasquale Striano Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, "G Gaslini" Institute, Genova, Italy Pediatric Neurology and Muscular Diseases Unit, IRCCS’ G Gaslini" Institute, Genova, Italy PubMed articlesGoogle scholar articles
  • Rikke Steensbjerre Møller Department of Epilepsy Genetics and Personalized Treatment, The Danish Epilepsy Centre Filadelfia, Dianalund, Denmark Institute for Regional Health Research, University of Southern Denmark, Odense, Denmark PubMed articlesGoogle scholar articles
  • Edward Cooper Department of Neurology, Baylor College of Medicine, Houston, Texas, USA PubMed articlesGoogle scholar articles
  • Sarah Weckhuysen Neurology Department, University Hospital Antwerp, Antwerp, Belgium Applied & Translational Neurogenomics Group, VIB-Center for Molecular Neurology, VIB, Antwerp, Belgium Translational Neuroscience Group, University of Antwerp, Antwerp, Belgium PubMed articlesGoogle scholar articles
  1. Correspondence to Prof. Dr. Sarah Weckhuysen; sarah.weckhuysen{at}uantwerpen.vib.be
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Citation

Boets S, Johannesen KM, Destree A, et al
Adult phenotype of KCNQ2 encephalopathy
Journal of Medical Genetics 2022;59:528-535.

Publication history

  • Received September 9, 2020
  • Revised March 2, 2021
  • Accepted March 10, 2021
  • First published April 2, 2021.
Online issue publication 
November 15, 2022

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© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.