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
[FOXG1, a new gene responsible for the congenital form of Rett syndrome].
Roche-Martinez A et al.
Revista De Neurologia, 2011
Novel FOXG1 mutations associated with the congenital variant of Rett syndrome.
Mencarelli MA et al.
Journal of Medical Genetics, 2010
A case of congenital Rett variant in a Chinese patient caused by a FOXG1 mutation.
Niu Y et al.
Annals of Saudi Medicine, 0
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