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Epilepsy phenotype in individuals with chromosomal duplication encompassing FGF12.
Willemsen, Marjolein H; Goel, Himanshu; Verhoeven, Judith S; Braakman, Hilde M H; de Leeuw, Nicole; Freeth, Alison; Minassian, Berge A.
Afiliación
  • Willemsen MH; Department of Clinical Genetics Maastricht University Medical Centre Maastricht The Netherlands.
  • Goel H; Department of Human Genetics Radboud University Medical Center Nijmegen The Netherlands.
  • Verhoeven JS; Donders Institute for Brain Cognition and Behaviour Radboud University Nijmegen The Netherlands.
  • Braakman HMH; Hunter Genetics Waratah NSW Australia.
  • de Leeuw N; University of Newcastle Callaghan NSW Australia.
  • Freeth A; Department of Neurology Academic Center for Epileptology Kempenhaeghe and Maastricht UMC+ Heeze The Netherlands.
  • Minassian BA; Donders Institute for Brain Cognition and Behaviour Radboud University Nijmegen The Netherlands.
Epilepsia Open ; 5(2): 301-306, 2020 Jun.
Article en En | MEDLINE | ID: mdl-32524056

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Epilepsia Open Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Epilepsia Open Año: 2020 Tipo del documento: Article