Novel FOXG1 mutations associated with the congenital variant of Rett syndrome.

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Published in J Med Genet on July 02, 2009

Authors

M A Mencarelli1, A Spanhol-Rosseto, R Artuso, D Rondinella, R De Filippis, N Bahi-Buisson, J Nectoux, R Rubinsztajn, T Bienvenu, A Moncla, B Chabrol, L Villard, Z Krumina, J Armstrong, A Roche, M Pineda, E Gak, F Mari, F Ariani, A Renieri

Author Affiliations

1: Medical Genetics, Molecular Biology Department, University of Siena, 53100 Siena, Italy.

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