Menin Deficiency Induces Autism-Like Behaviors by Regulating Foxg1 Transcription and Participates in Foxg1-Related Encephalopathy
Source: Advanced Science
Top caregiver concerns in Rett syndrome and related disorders: data from the US natural history study
Source: Journal of Neurodevelopmental Disorders
Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry
Source: Orphanet Journal of Rare Diseases
Comparison of evoked potentials across four related developmental encephalopathies
Source: Journal of Neurodevelopmental Disorders
The clinical and sleep manifestations in children with FOXG1 syndrome
Source: Autism Research
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