학술논문
FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects
Document Type
Article
Author
Cospain, A.; Rollier, P.; Odent, S.; Carre, W.; Bouvet, R.; Faoucher, M.; Dubourg, C.; Rivera-Barahona, A.; Gómez-Carmona, R.; Lapunzina, P.; Ruiz-Pérez, V.L.; Pérez-Jurado, L.A.; Dumontet, E.; Tarte, K.; Gener, B.; Bailleul-Forestier, I.; Meyts, I.; Moens, L.; Delafontaine, S.; Jouret, G.; Isidor, B.; Besnard, T.; Cogne, B.; Brewer, C.; Wuyts, W.; Keung Lam, W.W.; Van Den Bogaert, K.; Boogaerts, A.; Devriendt, K.; Scalais, E.; Guissard, C.; Pasquier, L.
Source
In: Genetics in Medicine . (Genetics in Medicine, December 2022, 24(12):2475-2486)
Subject
Language
English
ISSN
15300366
10983600
10983600