Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant

  • Nadia Bahi-Buisson, Juliette Nectoux, Benoit Girard, Hilde Van Esch, Thomy De Ravel, Nathalie Boddaert, Perrine Plouin, Marlene Rio, Yann Fichou, Jamel Chelly, Thierry Bienvenu
  • Neurogenetics, October 2009, Springer Science + Business Media
  • DOI: 10.1007/s10048-009-0220-2

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http://dx.doi.org/10.1007/s10048-009-0220-2