Novel molecular pathways elicited by mutant FGFR2 may account for brain abnormalities in Apert syndrome.

by Erika Yeh, Roberto D Fanganiello, Daniele Y Sunaga, Xueyan Zhou, Gregory Holmes, Katia M Rocha, Nivaldo Alonso, Hamilton Matushita, Yingli Wang, Ethylin W Jabs, Maria Rita Passos-Bueno
Published 2013-01-01