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Rett syndrome due to mutation in the MECP2 gene and electroencephalographic findings.

Arquivos de neuro-psiquiatria - 1 Aug 2024

Carvalho Marta Rodrigues de, Cavalcante Thiago Toscano, Oliveira Pedro Sudbrack, Naves Pedro Vicente Ferreira, Cunha Paulo Emidio Lobão

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PMID: 39074906
DOI: 10.1055/s-0044-1787801

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