FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring.
J Neurodev Disord. 2021 Apr 23;13(1):18. doi: 10.1186/s11689-021-09358-1.
J Neurodev Disord. 2021.
PMID: 33892622
Free PMC article.
Review.
FOXP1 syndrome is a neurodevelopmental disorder caused by mutations or deletions that disrupt the forkhead box protein 1 (FOXP1) gene, which encodes a transcription factor important for the early development of many organ systems, including the brain. ...Here, we pr …
FOXP1 syndrome is a neurodevelopmental disorder caused by mutations or deletions that disrupt the forkhead box protein 1 (FOXP1 …