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TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function.
Ba, Wei; Yan, Yan; Reijnders, Margot R F; Schuurs-Hoeijmakers, Janneke H M; Feenstra, Ilse; Bongers, Ernie M H F; Bosch, Daniëlle G M; De Leeuw, Nicole; Pfundt, Rolph; Gilissen, Christian; De Vries, Petra F; Veltman, Joris A; Hoischen, Alexander; Mefford, Heather C; Eichler, Evan E; Vissers, Lisenka E L M; Nadif Kasri, Nael; De Vries, Bert B A.
Afiliação
  • Ba W; Department of Human Genetics, Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, PO Box 9101, 6500 HB Nijmegen, The Netherlands.
  • Yan Y; Department of Neuroscience, UCONN Health Center, Farmington, CT 06030, USA.
  • Reijnders MR; Department of Human Genetics.
  • Schuurs-Hoeijmakers JH; Department of Human Genetics.
  • Feenstra I; Department of Human Genetics.
  • Bongers EM; Department of Human Genetics.
  • Bosch DG; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, PO Box 9101, 6500 HB Nijmegen, The Netherlands, Bartiméus, Institute for the Visually Impaired, Zeist, The Netherlands and.
  • De Leeuw N; Department of Human Genetics.
  • Pfundt R; Department of Human Genetics.
  • Gilissen C; Department of Human Genetics.
  • De Vries PF; Department of Human Genetics.
  • Veltman JA; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, PO Box 9101, 6500 HB Nijmegen, The Netherlands, Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Hoischen A; Department of Human Genetics.
  • Mefford HC; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA.
  • Eichler EE; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA, Howard Hughes Medical Institute, Seattle, WA 98195, USA.
  • Vissers LE; Department of Human Genetics.
  • Nadif Kasri N; Department of Human Genetics, Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, PO Box 9101, 6500 HB Nijmegen, The Netherlands, bert.devries@radboudumc.nl n.nadif@donders.ru.nl.
  • De Vries BB; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, PO Box 9101, 6500 HB Nijmegen, The Netherlands, bert.devries@radboudumc.nl n.nadif@donders.ru.nl.
Hum Mol Genet ; 25(5): 892-902, 2016 Mar 01.
Article em En | MEDLINE | ID: mdl-26721934
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Agitação Psicomotora / Transtorno Autístico / Sinapses / Proteínas Serina-Treonina Quinases / Fatores de Troca do Nucleotídeo Guanina / Deficiência Intelectual / Mutação / Neurônios Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Animals / Child / Female / Humans / Male Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Agitação Psicomotora / Transtorno Autístico / Sinapses / Proteínas Serina-Treonina Quinases / Fatores de Troca do Nucleotídeo Guanina / Deficiência Intelectual / Mutação / Neurônios Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Animals / Child / Female / Humans / Male Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda