학술논문
FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects
Document Type
Journal
Author
Cospain, Auriane; Rivera-Barahona, Ana; Dumontet, Erwan; Gener, Blanca; Bailleul-Forestier, Isabelle; Meyts, Isabelle; Jouret, Guillaume; Isidor, Bertrand; Brewer, Carole; Wuyts, Wim; Moens, Leen; Delafontaine, Selket; Lam, Wayne Wing Keung; Van den Bogaert, Kris; Boogaerts, Anneleen; Scalais, Emmanuel; Besnard, Thomas; Cogne, Benjamin; Guissard, Christophe; Rollier, Paul; Carre, Wilfrid; Bouvet, Regis; Tarte, Karin; Gomez-Carmona, Ricardo; Lapunzina, Pablo; Odent, Sylvie; Faoucher, Marie; Dubourg, Christele; Ruiz-Perez, Victor L.; Devriendt, Koen; Pasquier, Laurent; Perez-Jurado, Luis A.
Source
Subject
Language
English
ISSN
15300366