Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry
Source: Orphanet Journal of Rare Diseases
The clinical and sleep manifestations in children with FOXG1 syndrome
Source: Autism Research
Genotyping FOXG1 mutations in patients with clinical evidence of the FOXG1 syndrome
Source: Molecular Syndromology
Involvement of Mitochondrial Dysfunction in FOXG1 Syndrome
Source: Genes
Phenotypic overlap between pyruvate dehydrogenase complex deficiency and FOXG1 syndrome
Source: Clinical Case Reports
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