Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant.
Bahi-Buisson N; Nectoux J; Girard B; Van Esch H; De Ravel T; Boddaert N; Plouin P; Rio M; Fichou Y; Chelly J; Bienvenu T; Neurogenetics, 2010, vol. 11, issue 2, p 241, ISSN 13646753. ISBN 13646753.

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