FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring

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 a transcription factor important for the early development of many organ systems, including the brain. Numerous clinical studies have elucidat...

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Bibliographic Details
Main Authors: Reymundo Lozano, Catherine Gbekie, Paige M. Siper, Shubhika Srivastava, Jeffrey M. Saland, Swathi Sethuram, Lara Tang, Elodie Drapeau, Yitzchak Frank, Joseph D. Buxbaum, Alexander Kolevzon
Format: Article
Language:English
Published: BMC 2021-04-01
Series:Journal of Neurodevelopmental Disorders
Subjects:
FOXP1
Forkhead box protein 1
ASD
Autism spectrum disorder
FOXP1 syndrome
Online Access:https://doi.org/10.1186/s11689-021-09358-1

Internet

https://doi.org/10.1186/s11689-021-09358-1

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