Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.

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🔗 View Article (PMID 27933109)

Published in J Neurodev Disord on November 28, 2016

Authors

Sara B Estruch1, Sarah A Graham1, Swathi M Chinnappa1, Pelagia Deriziotis1, Simon E Fisher1,2

Author Affiliations

1: Language and Genetics Department, Max Planck Institute for Psycholinguistics, Wundtlaan 1, 6525 XD Nijmegen, the Netherlands.
2: Donders Institute for Brain, Cognition and Behaviour, Radboud University, 6525 EN Nijmegen, the Netherlands.

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