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Amedeo Smart

Independent Medical Education


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Mazel B, Delanne J, Garde A, Racine C, et al. FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development. Am J Med Genet B Neuropsychiatr Genet 2024 Mar 8:e32970.
PMID: 38459409


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