Your browser doesn't support javascript.
loading
Somatic mutation: The hidden genetics of brain malformations and focal epilepsies.
Ye, Zimeng; McQuillan, Lara; Poduri, Annapurna; Green, Timothy E; Matsumoto, Naomichi; Mefford, Heather C; Scheffer, Ingrid E; Berkovic, Samuel F; Hildebrand, Michael S.
Afiliação
  • Ye Z; Department of Medicine (Austin Hospital), University of Melbourne, Heidelberg, Victoria, Australia.
  • McQuillan L; Department of Medicine (Austin Hospital), University of Melbourne, Heidelberg, Victoria, Australia.
  • Poduri A; Epilepsy Genetics Program, Department of Neurology, Boston Children's Hospital, and Department of Neurology, Harvard Medical School, Boston, MA, United States.
  • Green TE; Department of Medicine (Austin Hospital), University of Melbourne, Heidelberg, Victoria, Australia.
  • Matsumoto N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Mefford HC; Division of Genetic Medicine, Department of Pediatrics, University of Washington and Seattle Children's Hospital, Seattle, WA, United States.
  • Scheffer IE; Department of Medicine (Austin Hospital), University of Melbourne, Heidelberg, Victoria, Australia; Department of Pediatrics, University of Melbourne, Royal Children's Hospital, Parkville, Victoria, Australia; Department of Neurology, Royal Children's Hospital, Parkville, Victoria, Australia; Murdoc
  • Berkovic SF; Department of Medicine (Austin Hospital), University of Melbourne, Heidelberg, Victoria, Australia.
  • Hildebrand MS; Department of Medicine (Austin Hospital), University of Melbourne, Heidelberg, Victoria, Australia; Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia. Electronic address: michael.hildebrand@unimelb.edu.au.
Epilepsy Res ; 155: 106161, 2019 09.
Article em En | MEDLINE | ID: mdl-31295639
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epilepsias Parciais / Malformações do Desenvolvimento Cortical / Mutação Limite: Humans Idioma: En Revista: Epilepsy Res Assunto da revista: CEREBRO / NEUROLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Austrália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epilepsias Parciais / Malformações do Desenvolvimento Cortical / Mutação Limite: Humans Idioma: En Revista: Epilepsy Res Assunto da revista: CEREBRO / NEUROLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Austrália