Behavioral Phenotypes of Foxg1 Heterozygous Mice
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DOI: 10.3389/fphar.2022.927296
Abstract: 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… read more here.
Keywords: heterozygous mice; behavioral phenotypes; human individuals; foxg1 heterozygous ... See more keywords