Associated Papers
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders.
Estruch SB et al.
Human Molecular Genetics, 2018
FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum.
Reuter MS et al.
Journal of Medical Genetics, 2017
Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.
Estruch SB et al.
Journal of Neurodevelopmental Disorders, 2016
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