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SCN1A variants associated with sudden infant death syndrome.
Brownstein, Catherine A; Goldstein, Richard D; Thompson, Christopher H; Haynes, Robin L; Giles, Emma; Sheidley, Beth; Bainbridge, Matthew; Haas, Elisabeth A; Mena, Othon J; Lucas, Jonathan; Schaber, Bethann; Holm, Ingrid A; George, Alfred L; Kinney, Hannah C; Poduri, Annapurna H.
Afiliação
  • Brownstein CA; Robert's Program on Sudden Death in Pediatrics, Boston Children's Hospital, Boston, MA, USA.
  • Goldstein RD; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA, USA.
  • Thompson CH; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
  • Haynes RL; Robert's Program on Sudden Death in Pediatrics, Boston Children's Hospital, Boston, MA, USA.
  • Giles E; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
  • Sheidley B; Department of Medicine, Division of General Pediatrics, Boston Children's Hospital, Boston, MA, USA.
  • Bainbridge M; Department of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Haas EA; Robert's Program on Sudden Death in Pediatrics, Boston Children's Hospital, Boston, MA, USA.
  • Mena OJ; Department of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.
  • Lucas J; Robert's Program on Sudden Death in Pediatrics, Boston Children's Hospital, Boston, MA, USA.
  • Schaber B; Department of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.
  • Holm IA; Epilepsy Genetics Program, Department of Neurology, Boston Children's Hospital, Boston, MA, USA.
  • George AL; The Genomics Institute, Rady Children's Hospital, San Diego, CA, USA.
  • Kinney HC; Department of Pathology, Rady Children's Hospital-San Diego, San Diego, CA, USA.
  • Poduri AH; Office of the Medical Examiner, County of San Diego Medical Examiner's Office, San Diego, CA, USA.
Epilepsia ; 59(4): e56-e62, 2018 04.
Article em En | MEDLINE | ID: mdl-29601086
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Morte Súbita do Lactente / Variação Genética / Canal de Sódio Disparado por Voltagem NAV1.1 Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Infant Idioma: En Revista: Epilepsia Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos
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: Morte Súbita do Lactente / Variação Genética / Canal de Sódio Disparado por Voltagem NAV1.1 Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Infant Idioma: En Revista: Epilepsia Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos