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      A functional genetic link between distinct developmental language disorders.

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          Abstract

          Rare mutations affecting the FOXP2 transcription factor cause a monogenic speech and language disorder. We hypothesized that neural pathways downstream of FOXP2 influence more common phenotypes, such as specific language impairment.

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          Author and article information

          Journal
          N Engl J Med
          The New England journal of medicine
          Massachusetts Medical Society
          1533-4406
          0028-4793
          Nov 27 2008
          : 359
          : 22
          Affiliations
          [1 ] Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
          Article
          NEJMoa0802828 NIHMS140850
          10.1056/NEJMoa0802828
          2756409
          18987363
          84f2150e-1e80-4b3f-a2ce-e402f7da6878
          2008 Massachusetts Medical Society
          History

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