Related Experiment Video
Updated: Jun 18, 2025

07:44
An Electrochemiluminescence-Based Assay for MeCP2 Protein Variants
Published on: May 22, 2020
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Rett syndrome due to mutation in the MECP2 gene and electroencephalographic findings
Marta Rodrigues de Carvalho1, Thiago Toscano Cavalcante1, Pedro Sudbrack Oliveira1
1Universidade de Brasília, Hospital Universitário de Brasília (HUB), Setor de Neurofisiologia Clínica, Brasília DF, Brazil.
Arquivos De Neuro-Psiquiatria
|July 29, 2024
Abstract
No abstract available in PubMed .

