Revisiting the phenotype associated withFOXG1mutations: two...

Revisiting the phenotype associated withFOXG1mutations: 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
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Volume:
11
Language:
english
Pages:
9
DOI:
10.1007/s10048-009-0220-2
Date:
May, 2010
File:
PDF, 485 KB
english, 2010
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