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Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder.
Sollis, Elliot; Graham, Sarah A; Vino, Arianna; Froehlich, Henning; Vreeburg, Maaike; Dimitropoulou, Danai; Gilissen, Christian; Pfundt, Rolph; Rappold, Gudrun A; Brunner, Han G; Deriziotis, Pelagia; Fisher, Simon E.
Afiliação
  • Sollis E; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen 6525 XD, The Netherlands.
  • Graham SA; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen 6525 XD, The Netherlands.
  • Vino A; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen 6525 XD, The Netherlands.
  • Froehlich H; Department of Human Molecular Genetics, Heidelberg University, Heidelberg 69120, Germany.
  • Vreeburg M; Department of Clinical Genetics and School for Oncology & Developmental Biology (GROW), Maastricht UMC, Maastricht 6202 AZ, The Netherlands.
  • Dimitropoulou D; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen 6525 XD, The Netherlands.
  • Gilissen C; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Nijmegen 6500 HB, The Netherlands.
  • Pfundt R; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Nijmegen 6500 HB, The Netherlands.
  • Rappold GA; Department of Human Molecular Genetics, Heidelberg University, Heidelberg 69120, Germany, Interdisciplinary Center of Neurosciences (IZN), Heidelberg University, Heidelberg 69120, Germany and.
  • Brunner HG; Department of Clinical Genetics and School for Oncology & Developmental Biology (GROW), Maastricht UMC, Maastricht 6202 AZ, The Netherlands, Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Nijmegen 6500 HB, The Netherlands.
  • Deriziotis P; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen 6525 XD, The Netherlands, pelagia.derizioti@mpi.nl simon.fisher@mpi.nl.
  • Fisher SE; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen 6525 XD, The Netherlands, Donders Institute for Brain, Cognition and Behaviour, Nijmegen 6525 EN, The Netherlands pelagia.derizioti@mpi.nl simon.fisher@mpi.nl.
Hum Mol Genet ; 25(3): 546-57, 2016 Feb 01.
Article em En | MEDLINE | ID: mdl-26647308
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Deficiências do Desenvolvimento / Mutação de Sentido Incorreto / Fatores de Transcrição Forkhead / Hipertelorismo / Transtornos do Desenvolvimento da Linguagem / Deficiência Intelectual Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Adolescent / 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 Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Deficiências do Desenvolvimento / Mutação de Sentido Incorreto / Fatores de Transcrição Forkhead / Hipertelorismo / Transtornos do Desenvolvimento da Linguagem / Deficiência Intelectual Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Adolescent / 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