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

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

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Bahi-Buisson, Nadia | Nectoux, Juliette | Girard, Benoit | van Esch, Hilde | de Ravel, Thomy | Boddaert, Nathalie | Plouin, Perrine | Rio, Marlene | Fichou, Yann | Chelly, Jamel | Bienvenu, Thierry

Edité par CCSD ; Springer Verlag -

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Langue: en

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