FoxP1 orchestration of ASD-relevant signaling pathways in the striatum.

Abstract

Mutations in the transcription factor Forkhead box p1 (FOXP1) are causative for neurodevelopmental disorders such as autism. However, the function of FOXP1 within the brain remains largely uncharacterized. Here, we identify the gene expression program regulated by FoxP1 in both human neural cells and patient-relevant heterozygous Foxp1 mouse brains. We… (More)
DOI: 10.1101/gad.267989.115

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