Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.
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| Title: | Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment. |
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| Authors: | Villanueva P; Human Genetics Program, Institute of Biomedical Sciences (ICBM), Faculty of Medicine, University of Chile, Santiago, Chile; School of Speech and Hearing Therapy, Faculty of Medicine, University of Chile, Santiago, Chile; Department of Child and Dental Maxillary Orthopedics, Faculty of Dentistry, University of Chile, Santiago, Chile; Doctoral Program of Psychology, Graduate School, University of Granada, Granada, Spain., Nudel R; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom., Hoischen A; Department of Human Genetics, Radboud Institute for Molecular Life Sciences and Donders Centre for Neuroscience, Radboud University Medical Center, Nijmegen, the Netherlands., Fernández MA; School of Speech and Hearing Therapy, Faculty of Medicine, University of Chile, Santiago, Chile., Simpson NH; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom., Gilissen C; Department of Human Genetics, Radboud Institute for Molecular Life Sciences and Donders Centre for Neuroscience, Radboud University Medical Center, Nijmegen, the Netherlands., Reader RH; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom., Jara L; Human Genetics Program, Institute of Biomedical Sciences (ICBM), Faculty of Medicine, University of Chile, Santiago, Chile., Echeverry MM; Grupo de Citogenetica, Filogenia y Evolucion de las Poblaciones, Facultades de Ciencias y de Ciencias de la Salud, Universidad del Tolima, Ibague, Colombia., Francks C; Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, the Netherlands., Baird G; Newcomen Centre, the Evelina Children's Hospital, London, United Kingdom., Conti-Ramsden G; School of Psychological Sciences, University of Manchester, Manchester, United Kingdom., O'Hare A; Department of Reproductive and Developmental Sciences, University of Edinburgh, Edinburgh, United Kingdom., Bolton PF; Departments of Child & Adolescent Psychiatry & Social Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, London, United Kingdom., Hennessy ER; University Child Health and DMDE, University of Aberdeen, Aberdeen, United Kingdom., Palomino H; Department of Child and Dental Maxillary Orthopedics, Faculty of Dentistry, University of Chile, Santiago, Chile., Carvajal-Carmona L; Grupo de Citogenetica, Filogenia y Evolucion de las Poblaciones, Facultades de Ciencias y de Ciencias de la Salud, Universidad del Tolima, Ibague, Colombia; UC Davis Genome Center, Department of Biochemistry and Molecular Medicine, School of Medicine, University of California Davis, Davis, California, United States of America., Veltman JA; Department of Human Genetics, Radboud Institute for Molecular Life Sciences and Donders Centre for Neuroscience, Radboud University Medical Center, Nijmegen, the Netherlands., Cazier JB; Department of Oncology, University of Oxford, Oxford, United Kingdom; Centre for Computational Biology, University of Birmingham, Edgbaston, United Kingdom., De Barbieri Z; School of Speech and Hearing Therapy, Faculty of Medicine, University of Chile, Santiago, Chile., Fisher SE; Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, the Netherlands., Newbury DF; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom; St Johns College, University of Oxford, Oxford, United Kingdom. |
| Corporate Authors: | SLI Consortium |
| Source: | PLoS genetics [PLoS Genet] 2015 Mar 17; Vol. 11 (3), pp. e1004925. Date of Electronic Publication: 2015 Mar 17 (Print Publication: 2015). |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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