Associated Papers
Functional defects in FOXG1 variants predict the severity of brain anomalies in FOXG1 syndrome.
Lin TY et al.
Molecular Psychiatry, 2025
Genetic diagnostic outcomes from a 10-year research programme in autism in Aotearoa New Zealand.
Musgrave SM et al.
Journal of the Royal Society of New Zealand, 2025
40756852 (PubMed )
Supplement: TNZR_A_2394128_SM9470.xlsx › Sheet1
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
Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice.
Pringsheim M et al.
Annals of Clinical and Translational Neurology, 2019
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