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The -413C > G substitution in the promoter of the FMR1 gene is not associated with the fragile X syndrome phenotype
Marina Grasso, Massimiliano Cecconi, Stefania Boni, Francesca Forzano, Maurizio Barbaresi, Luigi Memo, Lucia Perroni, Francesca Faravelli, Emilio Di MariaVolume:
24
Année:
2010
Langue:
english
DOI:
10.1016/j.mcp.2009.10.006
Fichier:
PDF, 322 KB
english, 2010