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BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures.
Scheffer, Ingrid E; Boysen, Katja E; Schneider, Amy L; Myers, Candace T; Mehaffey, Michele G; Rochtus, Anne M; Yuen, Yuet-Ping; Ronen, Gabriel M; Chak, Wai Km; Gill, Deepak; Poduri, Annapurna; Mefford, Heather C.
Afiliação
  • Scheffer IE; Epilepsy Research Centre, Department of Medicine, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia.
  • Boysen KE; Florey Institute of Neuroscience and Mental Health, Heidelberg, Victoria, Australia.
  • Schneider AL; Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Myers CT; Department of Paediatrics, Royal Children's Hospital, Parkville, Victoria, Australia.
  • Mehaffey MG; Epilepsy Research Centre, Department of Medicine, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia.
  • Rochtus AM; Epilepsy Research Centre, Department of Medicine, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia.
  • Yuen YP; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA, USA.
  • Ronen GM; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA, USA.
  • Chak WK; Epilepsy Genetics Program, Department of Neurology, Boston Children's Hospital, Boston, MA, USA.
  • Gill D; Department of Neurology, Harvard Medical School, Boston, MA, USA.
  • Poduri A; Hong Kong Children's Hospital, Hong Kong.
  • Mefford HC; Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
Dev Med Child Neurol ; 62(9): 1096-1099, 2020 09.
Article em En | MEDLINE | ID: mdl-31868227
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Convulsões / Encefalopatias / Proteínas Nucleares / Epilepsia Tipo de estudo: Prognostic_studies Limite: Humans / Newborn Idioma: En Revista: Dev Med Child Neurol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Austrália País de publicação: Reino Unido
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Convulsões / Encefalopatias / Proteínas Nucleares / Epilepsia Tipo de estudo: Prognostic_studies Limite: Humans / Newborn Idioma: En Revista: Dev Med Child Neurol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Austrália País de publicação: Reino Unido