L’ETUDE MOLECULAIRE DU SYNDROME DE RETT (Aproposde08cas)
Rett syndrome is a genetic disease caused nearly 80% in typical cases and 30% of atypical forms by mutations in the MECP2 gene located in Xq28, which is a transcriptional repressor. Loss the function of the MeCP2 protein could cause overexpression of certain genes, which would be detrimental to the development of the central nervous […]