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Rôle de MECP2 au cours du développement précoce du cortex cérébral chez les primates
MECP2 (protéine 2 de liaison méthyle CpG) est un gène situé sur le chromosome Xq28 chez l'humain. MECP2 est largement connu pour être associé à deux principaux troubles neurologiques sévères : le syndrome de Rett (RTT) et le syndrome de duplication de MECP2 (MDS), caractérisés par une apparition des
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