Cite
HARVARD Citation
Reuter, M. et al. (2017). FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum. Journal of medical genetics. 54 (1), pp. 64-72. [Online].
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Reuter, M. et al. (2017). FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum. Journal of medical genetics. 54 (1), pp. 64-72. [Online].