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Journal Article

Functional characterization of rare FOXP2 variants in neurodevelopmental disorder

MPS-Authors
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Estruch,  Sara Busquets
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society, Nijmegen, NL;
International Max Planck Research School for Language Sciences, MPI for Psycholinguistics, Max Planck Society;

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Graham,  Sarah A.
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society, Nijmegen, NL;

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Deriziotis,  Pelagia
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society, Nijmegen, NL;

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Fisher,  Simon E.
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society, Nijmegen, NL;
Donders Institute for Brain, Cognition and Behaviour, External Organizations;

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Estruch_etal_2016.pdf
(Publisher version), 3MB

Citation

Estruch, S. B., Graham, S. A., Chinnappa, S. M., Deriziotis, P., & Fisher, S. E. (2016). Functional characterization of rare FOXP2 variants in neurodevelopmental disorder. Journal of Neurodevelopmental Disorders, 8: 44. doi:10.1186/s11689-016-9177-2.


Cite as: http://hdl.handle.net/11858/00-001M-0000-002B-B91A-D
Abstract
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