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A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.
Merner, Nancy; Forgeot d'Arc, Baudouin; Bell, Scott C; Maussion, Gilles; Peng, Huashan; Gauthier, Julie; Crapper, Liam; Hamdan, Fadi F; Michaud, Jacques L; Mottron, Laurent; Rouleau, Guy A; Ernst, Carl.
Afiliación
  • Merner N; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.
  • Forgeot d'Arc B; Department of Human Genetics, McGill University, Montreal, Quebec, Canada.
  • Bell SC; Montreal Neurological Institute, Montreal, Quebec, Canada.
  • Maussion G; Riviere-des-Prairies Hospital, University of Montreal, Montreal, Quebec, Canada.
  • Peng H; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.
  • Gauthier J; Douglas Hospital Research Institute, Montreal, Quebec, Canada.
  • Crapper L; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.
  • Hamdan FF; Douglas Hospital Research Institute, Montreal, Quebec, Canada.
  • Michaud JL; Douglas Hospital Research Institute, Montreal, Quebec, Canada.
  • Mottron L; CHU Sainte-Justine Research Center, University of Montreal, Montreal, Quebec, Canada.
  • Rouleau GA; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.
  • Ernst C; CHU Sainte-Justine Research Center, University of Montreal, Montreal, Quebec, Canada.
Am J Med Genet A ; 170A(5): 1225-35, 2016 May.
Article en En | MEDLINE | ID: mdl-26789910
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Esquizofrenia / Factores de Transcripción / Proteínas de Unión al ADN / Trastorno del Espectro Autista Tipo de estudio: Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Canadá
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Esquizofrenia / Factores de Transcripción / Proteínas de Unión al ADN / Trastorno del Espectro Autista Tipo de estudio: Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Canadá