Associated Papers
Autism with dysphasia accompanied by mental retardation caused by FOXP1 exon deletion: A case report.
Lin SZ et al.
World Journal of Clinical Cases, 2021
An Autism-Related, Nonsense Foxp1 Mutant Induces Autophagy and Delays Radial Migration of the Cortical Neurons.
Li X et al.
Cerebral Cortex (new York, N.y. : 1991), 2019
Variation in a range of mTOR-related genes associates with intracranial volume and intellectual disability.
Reijnders MRF et al.
Nature Communications, 2017
29051493 (PubMed )
Supplement: 41467_2017_933_MOESM5_ESM.xlsx › All_de_novo_mutations
FOXP1-related intellectual disability syndrome: a recognisable entity.
Meerschaut I et al.
Journal of Medical Genetics, 2017
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder.
Sollis E et al.
Human Molecular Genetics, 2016
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