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Clinical Course of Six Children With GNAO1 Mutations Causing a Severe and Distinctive Movement Disorder.
Ananth, Amitha L; Robichaux-Viehoever, Amy; Kim, Young-Min; Hanson-Kahn, Andrea; Cox, Rachel; Enns, Gregory M; Strober, Jonathan; Willing, Marcia; Schlaggar, Bradley L; Wu, Yvonne W; Bernstein, Jonathan A.
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  • Ananth AL; Department of Pediatrics, Stanford University, Stanford, California. Electronic address: Amitha@stanford.edu.
  • Robichaux-Viehoever A; Department of Neurology, University of California San Francisco, San Francisco, California; Department of Pediatrics, University of California San Francisco, San Francisco, California. Electronic address: amy.viehoever@UCSF.edu.
  • Kim YM; Department of Neurology, Washington University in St. Louis School of Medicine, St. Louis, Missouri.
  • Hanson-Kahn A; Department of Pediatrics, Stanford University, Stanford, California; Department of Genetics, Stanford University, Stanford, California.
  • Cox R; Department of Pediatrics, Stanford University, Stanford, California.
  • Enns GM; Department of Pediatrics, Stanford University, Stanford, California.
  • Strober J; Department of Neurology, University of California San Francisco, San Francisco, California; Department of Pediatrics, University of California San Francisco, San Francisco, California.
  • Willing M; Department of Pediatrics, Washington University in St. Louis School of Medicine, St. Louis, Missouri.
  • Schlaggar BL; Department of Neurology, Washington University in St. Louis School of Medicine, St. Louis, Missouri; Department of Pediatrics, Washington University in St. Louis School of Medicine, St. Louis, Missouri; Department of Anatomy and Neurobiology, Washington University in St. Louis School of Medicine, St
  • Wu YW; Department of Neurology, University of California San Francisco, San Francisco, California; Department of Pediatrics, University of California San Francisco, San Francisco, California.
  • Bernstein JA; Department of Pediatrics, Stanford University, Stanford, California.
Pediatr Neurol ; 59: 81-4, 2016 06.
Article en En | MEDLINE | ID: mdl-27068059
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Subunidades alfa de la Proteína de Unión al GTP Gi-Go / Trastornos del Movimiento Tipo de estudio: Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Pediatr Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2016 Tipo del documento: Article
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Subunidades alfa de la Proteína de Unión al GTP Gi-Go / Trastornos del Movimiento Tipo de estudio: Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Pediatr Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2016 Tipo del documento: Article