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