Associated Papers
FOXG1-Related Syndrome: From Clinical to Molecular Genetics and Pathogenic Mechanisms.
Wong LC et al.
International Journal of Molecular Sciences, 2019
31454984 (PubMed )
Supplement: ijms-20-04176-s001.pdf
Delineation of the movement disorders associated with FOXG1 mutations.
Papandreou A et al.
Neurology, 2016
Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis.
Trump N et al.
Journal of Medical Genetics, 2016
Familial recurrences of FOXG1-related disorder: Evidence for mosaicism.
McMahon KQ et al.
American Journal of Medical Genetics. Part A, 2015
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