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Original article
FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum

Authors

  1. Correspondence to Dr Christiane Zweier, Institute of Human Genetics, Friedrich-Alexander-University Erlangen-Nürnberg, Schwabachanlage 10, Erlangen 91054, Germany; christiane.zweier{at}uk-erlangen.de
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Citation

Reuter MS, Riess A, Moog U, et al
FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum

Publication history

  • Received June 9, 2016
  • Revised July 31, 2016
  • Accepted August 1, 2016
  • First published August 29, 2016.
Online issue publication 
January 06, 2017

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