FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring
Abstract FOXP1 syndrome is a neurodevelopmental disorder caused by mutations or deletions that disrupt the forkhead box protein 1 (FOXP1) gene, which encodes Men Care a transcription factor important for the early development of many organ systems, including the brain.Numerous clinical studies have elucidated the role of FOXP1 in neurodevelopment a