Pharmacoresistant epilepsy associated with mutations in the KCNB1 and RELN genes. A case report
Authors
Adamantios Katerelos
Department of Neurology, “Karamandaneio”, Children’s Hospital, Patra, Greece
Nikolaos Zagkos
Department of Neurology, “Karamandaneio”, Children’s Hospital, Patra, Greece
Dimitra Alexopoulou
Department of Neurology, “Karamandaneio”, Children’s Hospital, Patra, Greece
Stella Mouskou
Department of Neurology, “P & A Kyriakou”, Children’s Hospital, Athens, Greece
Anastasia Korona
Department of Neurology, “P & A Kyriakou”, Children’s Hospital, Athens, Greece
Emmanouil Manolakos
Access To Genome, Clinical Laboratory Genetics, Athens-Thessaloniki, Greece
Language: English
Page range: 73 - 77
Submitted on: Jul 31, 2020
Accepted on: Oct 15, 2020
Published on: Nov 25, 2020
Published by: The Foundation of Epileptology
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Related subjects:
© 2020 Adamantios Katerelos, Nikolaos Zagkos, Dimitra Alexopoulou, Stella Mouskou, Anastasia Korona, Emmanouil Manolakos, published by The Foundation of Epileptology
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.