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The -413C > G substitution in the promoter of the FMR1 gene is not associated with the fragile X syndrome phenotype

✍ Scribed by Marina Grasso; Massimiliano Cecconi; Stefania Boni; Francesca Forzano; Maurizio Barbaresi; Luigi Memo; Lucia Perroni; Francesca Faravelli; Emilio Di Maria

Book ID: 116736045
Publisher: Elsevier Science
Year: 2010
Tongue: English
Weight: 322 KB
Volume: 24
Category: Article
ISSN: 0890-8508
DOI: 10.1016/j.mcp.2009.10.006

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