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    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. (2010). novel FOXG1 mutations associated with the congenital variant of Rett syndrome. Journal of medical genetics, 47(1), 49–53. http://access.bl.uk/ark:/81055/vdc_100135569067.0x00003e