Your browser doesn't support javascript.
loading
Haploinsufficiency of MeCP2-interacting transcriptional co-repressor SIN3A causes mild intellectual disability by affecting the development of cortical integrity.
Witteveen, Josefine S; Willemsen, Marjolein H; Dombroski, Thaís C D; van Bakel, Nick H M; Nillesen, Willy M; van Hulten, Josephus A; Jansen, Eric J R; Verkaik, Dave; Veenstra-Knol, Hermine E; van Ravenswaaij-Arts, Conny M A; Wassink-Ruiter, Jolien S Klein; Vincent, Marie; David, Albert; Le Caignec, Cedric; Schieving, Jolanda; Gilissen, Christian; Foulds, Nicola; Rump, Patrick; Strom, Tim; Cremer, Kirsten; Zink, Alexander M; Engels, Hartmut; de Munnik, Sonja A; Visser, Jasper E; Brunner, Han G; Martens, Gerard J M; Pfundt, Rolph; Kleefstra, Tjitske; Kolk, Sharon M.
Afiliação
  • Witteveen JS; Department of Molecular Animal Physiology, Donders Institute for Brain, Cognition and Behavior, Radboud University, Nijmegen, the Netherlands.
  • Willemsen MH; Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition and Behavior, Nijmegen, the Netherlands.
  • Dombroski TC; Department of Molecular Animal Physiology, Donders Institute for Brain, Cognition and Behavior, Radboud University, Nijmegen, the Netherlands.
  • van Bakel NH; Department of Molecular Animal Physiology, Donders Institute for Brain, Cognition and Behavior, Radboud University, Nijmegen, the Netherlands.
  • Nillesen WM; Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition and Behavior, Nijmegen, the Netherlands.
  • van Hulten JA; Department of Molecular Animal Physiology, Donders Institute for Brain, Cognition and Behavior, Radboud University, Nijmegen, the Netherlands.
  • Jansen EJ; Department of Molecular Animal Physiology, Donders Institute for Brain, Cognition and Behavior, Radboud University, Nijmegen, the Netherlands.
  • Verkaik D; Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition and Behavior, Nijmegen, the Netherlands.
  • Veenstra-Knol HE; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
  • van Ravenswaaij-Arts CM; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
  • Wassink-Ruiter JS; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
  • Vincent M; Centre Hospitalier Universitaire de Nantes, Service de Génétique Médicale, Nantes, France.
  • David A; Centre Hospitalier Universitaire de Nantes, Service de Génétique Médicale, Nantes, France.
  • Le Caignec C; Centre Hospitalier Universitaire de Nantes, Service de Génétique Médicale, Nantes, France.
  • Schieving J; Laboratoire de Physiopathologie de la Résorption Osseuse et Thérapie des Tumeurs Osseuses Primitives, Faculté de Médecine, INSERM UMRS 957, Nantes, France.
  • Gilissen C; Department of Neurology, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Foulds N; Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition and Behavior, Nijmegen, the Netherlands.
  • Rump P; Wessex Clinical Genetics Services, University Hospital Southampton National Health Service Foundation Trust, Princess Anne Hospital, Southampton, UK.
  • Strom T; Department of Human Genetics and Genomic Medicine, Faculty of Medicine, University of Southampton, Southampton, UK.
  • Cremer K; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
  • Zink AM; Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany.
  • Engels H; Institute of Human Genetics, Technische Universität München, Munich, Germany.
  • de Munnik SA; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Visser JE; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Brunner HG; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Martens GJ; Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition and Behavior, Nijmegen, the Netherlands.
  • Pfundt R; Department of Molecular Animal Physiology, Donders Institute for Brain, Cognition and Behavior, Radboud University, Nijmegen, the Netherlands.
  • Kleefstra T; Department of Neurology, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Kolk SM; Department of Neurology, Amphia Hospital Breda, Berda, the Netherlands.
Nat Genet ; 48(8): 877-87, 2016 08.
Article em En | MEDLINE | ID: mdl-27399968
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Córtex Cerebral / Proteína 2 de Ligação a Metil-CpG / Neurogênese / Haploinsuficiência / Deficiência Intelectual / Mutação Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Adolescent / Adult / Animals / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Nat Genet Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Córtex Cerebral / Proteína 2 de Ligação a Metil-CpG / Neurogênese / Haploinsuficiência / Deficiência Intelectual / Mutação Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Adolescent / Adult / Animals / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Nat Genet Ano de publicação: 2016 Tipo de documento: Article