(Q41937721)
Statements
Novel FOXG1 mutations associated with the congenital variant of Rett syndrome (English)
M A Mencarelli
A Spanhol-Rosseto
D Rondinella
R De Filippis
N Bahi-Buisson
J Nectoux
R Rubinsztajn
T Bienvenu
A Moncla
B Chabrol
Z Krumina
J Armstrong
A Roche
M Pineda