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

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 elucidated the ro...

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Detalles Bibliográficos
Autores principales: Lozano, Reymundo, Gbekie, Catherine, Siper, Paige M., Srivastava, Shubhika, Saland, Jeffrey M., Sethuram, Swathi, Tang, Lara, Drapeau, Elodie, Frank, Yitzchak, Buxbaum, Joseph D., Kolevzon, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8066957/
https://www.ncbi.nlm.nih.gov/pubmed/33892622
http://dx.doi.org/10.1186/s11689-021-09358-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8066957/
https://www.ncbi.nlm.nih.gov/pubmed/33892622
http://dx.doi.org/10.1186/s11689-021-09358-1

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