Behavioral and brain anatomical analysis of Foxg1 heterozygous mice

Behavioral and brain anatomical analysis of Foxg1 heterozygous mice

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FOXG1 Syndrome (FS) is a devastating neurodevelopmental disorder that is caused by a heterozygous loss-of-function (LOF) mutation of the FOXG1 gene, which encodes a transcriptional regulator important for telencephalic brain development. People with FS have marked developmental delays, impaired ambu...

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Bibliographic Details
Main Authors: Kirsty R. Erickson, Rebekah Farmer, Jonathan K. Merritt, Zeljka Miletic Lanaghan, Mark D. Does, Karthik Ramadass, Bennett A. Landman, Laurie E. Cutting, Jeffrey L. Neul
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2022-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555627/?tool=EBI

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555627/?tool=EBI

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