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De novo mutations in moderate or severe intellectual disability.
Hamdan, Fadi F; Srour, Myriam; Capo-Chichi, Jose-Mario; Daoud, Hussein; Nassif, Christina; Patry, Lysanne; Massicotte, Christine; Ambalavanan, Amirthagowri; Spiegelman, Dan; Diallo, Ousmane; Henrion, Edouard; Dionne-Laporte, Alexandre; Fougerat, Anne; Pshezhetsky, Alexey V; Venkateswaran, Sunita; Rouleau, Guy A; Michaud, Jacques L.
Afiliação
  • Hamdan FF; CHU Sainte-Justine Research Center, Montreal, Canada.
  • Srour M; CHU Sainte-Justine Research Center, Montreal, Canada; Division of Pediatric Neurology, Montreal Children's Hospital, Montreal, Canada.
  • Capo-Chichi JM; CHU Sainte-Justine Research Center, Montreal, Canada.
  • Daoud H; Montreal Neurological Institute, McGill University, Montreal, Canada.
  • Nassif C; CHU Sainte-Justine Research Center, Montreal, Canada.
  • Patry L; CHU Sainte-Justine Research Center, Montreal, Canada.
  • Massicotte C; CHU Sainte-Justine Research Center, Montreal, Canada.
  • Ambalavanan A; Montreal Neurological Institute, McGill University, Montreal, Canada.
  • Spiegelman D; Montreal Neurological Institute, McGill University, Montreal, Canada.
  • Diallo O; Montreal Neurological Institute, McGill University, Montreal, Canada.
  • Henrion E; Montreal Neurological Institute, McGill University, Montreal, Canada.
  • Dionne-Laporte A; Montreal Neurological Institute, McGill University, Montreal, Canada.
  • Fougerat A; CHU Sainte-Justine Research Center, Montreal, Canada.
  • Pshezhetsky AV; CHU Sainte-Justine Research Center, Montreal, Canada.
  • Venkateswaran S; Division of Neurology, Children's Hospital of Eastern Ontario, Ottawa, Canada.
  • Rouleau GA; Montreal Neurological Institute, McGill University, Montreal, Canada.
  • Michaud JL; CHU Sainte-Justine Research Center, Montreal, Canada; Department of Pediatrics and Department of Neurosciences, University of Montreal, Montreal, Canada.
PLoS Genet ; 10(10): e1004772, 2014 Oct.
Article em En | MEDLINE | ID: mdl-25356899
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epilepsia / Deficiência Intelectual Limite: Humans Idioma: En Ano de publicação: 2014 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epilepsia / Deficiência Intelectual Limite: Humans Idioma: En Ano de publicação: 2014 Tipo de documento: Article