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Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.

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Title: Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.
Authors: Chen XS; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands., Reader RH; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK., Hoischen A; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., Veltman JA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Department of Clinical Genetics, University of Maastricht, Maastricht, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Nijmegen, The Netherlands., Simpson NH; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK., Francks C; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Nijmegen, The Netherlands., Newbury DF; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.; Department of Biological and Medical Sciences, Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK., Fisher SE; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Nijmegen, The Netherlands.
Source: Scientific reports [Sci Rep] 2017 Apr 25; Vol. 7, pp. 46105. Date of Electronic Publication: 2017 Apr 25.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: <searchLink fieldCode="AU" term="%22Chen+XS%22">Chen XS</searchLink>; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Reader+RH%22">Reader RH</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.<br /><searchLink fieldCode="AU" term="%22Hoischen+A%22">Hoischen A</searchLink>; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Veltman+JA%22">Veltman JA</searchLink>; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Department of Clinical Genetics, University of Maastricht, Maastricht, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Simpson+NH%22">Simpson NH</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.<br /><searchLink fieldCode="AU" term="%22Francks+C%22">Francks C</searchLink>; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Newbury+DF%22">Newbury DF</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.; Department of Biological and Medical Sciences, Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Fisher+SE%22">Fisher SE</searchLink>; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Nijmegen, The Netherlands.
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