Novel FOXG1 mutations associated with the congenital variant of Rett syndrome.
Mencarelli, M. A.; Spanhol-Rosseto, A.; Artuso, R.; Rondinella, D.; De Filippis, R.; Bahi-Buisson, N.; Nectoux, J.; Rubinsztajn, R.; Bienvenu, T.; Moncla, A.; Chabrol, B.; Villard, L.; Krumina, Z.; Armstrong, J.; Roche, A.; Pineda, M.; Gak, E.; Mari, F.; Ariani, F.; Renieri, A.; Journal of Medical Genetics, 2010, vol. 47, issue 1, p 5, ISSN 00222593. ISBN 14686244.

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