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
The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathy.
Cellini E et al.
Developmental Medicine and Child Neurology, 2016
Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delay.
Fryssira H et al.
Molecular Cytogenetics, 2016
Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin-binding dynamics.
De Filippis R et al.
Clinical Genetics, 2012
FOXG1-Related Disorders: From Clinical Description to Molecular Genetics.
Florian C et al.
Molecular Syndromology, 2012
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