Associated Papers
FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development.
Mazel B et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2024
Identification of FOXG1 mutations in infantile hypotonia and postnatal microcephaly.
Jang HN et al.
Medicine, 2021
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