Associated Papers
Autism-like features and FOXP1 syndrome: A scoping review.
Stewart J et al.
Brain & Development, 2025
Pathogenic variation underlying rare diseases in an Arab population: Implications for screening programs.
Jain R et al.
Genetics in Medicine Open, 2025
40893834 (PubMed )
Supplement: mmc1.xlsx › Supplementary_Table_1
Case report: FOXP1 syndrome caused by a de novo splicing variant (c.1652+5 G>A) of the FOXP1 gene.
Chen M et al.
Frontiers in Genetics, 2022
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