We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleRevisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant.AuthorsBahi-Buisson, Nadia; Nectoux, Juliette; Girard, Benoit; Esch, Hilde; Ravel, Thomy; Boddaert, Nathalie; Plouin, Perrine; Rio, Marlene; Fichou, Yann; Chelly, Jamel; Bienvenu, ThierryPublicationNeurogenetics, 2010, Vol 11, Issue 2, p241ISSN1364-6745Publication typearticleDOI10.1007/s10048-009-0220-2