Behavioral Phenotypes of Foxg1 Heterozygous Mice

• Egile Nagusiak: Skyler Younger (Egilea), Sydney Boutros (Egilea), Francesca Cargnin (Egilea), Shin Jeon (Egilea), Jae W. Lee (Egilea), Soo-Kyung Lee (Egilea), Jacob Raber (Egilea)
• Formatua: Liburua
• Argitaratua: Frontiers Media S.A., 2022-06-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

FOXG1 syndrome (FS, aka a congenital variant of Rett syndrome) is a recently defined rare and devastating neurodevelopmental disorder characterized by various symptoms, including severe intellectual disability, autistic features, involuntary, and continuous jerky movements, feeding problems, sleep d...