Associated Papers
A comprehensive in silico analysis of the deleterious nonsynonymous SNPs of human FOXP2 protein.
Akter M et al.
Plos One, 2022
De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types.
Chen S et al.
Molecular Autism, 2020
33032641 (PubMed )
Supplement: 13229_2020_386_MOESM2_ESM.xlsx › Interaction_disruptions_proband
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
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