Novel FOXG1 mutations associated with the congenital variant of Rett syndrome

✍ Scribed by Mencarelli, M. A. (author);Spanhol-Rosseto, A. (author);Artuso, R. (author);Rondinella, D. (author);De Filippis, R. (author);Bahi-Buisson, N. (author);Nectoux, J. (author);Rubinsztajn, R. (author);Bienvenu, T. (author);Moncla, A. (author);Chabrol, B. (author);Villard, L. (author);Krumina, Z. (author);Armstrong, J. (author);Roche, A. (author);Pineda, M. (author);Gak, E. (author);Mari, F. (author);Ariani, F. (author);Renieri, A. (author)

• Book ID: 126898669
• Publisher: BMJ Publishing Group
• Year: 2009
• Tongue: English
• Weight: 421 KB
• Volume: 47
• Category: Article
• ISSN: 0022-2593
• DOI: 10.1136/jmg.2009.067884